Rare diseases that primarily involve the hematologic & blood system. Each links to its full hub — overview, specialists, clinical trials, medications and community.
How this grouping is built. These conditions are grouped by a clinical keyword match on the disease name — the same conservative classifier Tomeko uses to pick each hub’s system motif. It is a Tomeko working grouping, not an official Orphanet organ classification, and some conditions affect more than one system. Every condition is itself catalogued from NIH GARD (Genetic and Rare Diseases Information Center) and Orphanet (orpha.net), and each hub cites its own sources. Sorted A→Z by name · 764 conditions · last built 2026-08-30.
No conditions match that name. Try fewer letters, or browse all conditions.
A179
- A53 Diffuse Large B-Cell Lymphoma
- AA Amyloidosis
- AApoAIV Amyloidosis
- ABeta2M Amyloidosis
- ABri Amyloidosis
- Acquired Aplastic Anemia
- Acquired Coagulation Factor Deficiency
- Acquired Hemoglobin H Disease
- Acquired Hemoglobinopathy
- Acquired Hemophilia
- Acquired Hemophilia B
- Acquired Polycythemia
- Acquired Polycythemia Vera
- Acquired Secondary Polycythemia
- Acquired Thrombotic Thrombocytopenic Purpura
- Acroerythrokeratoderma
- ACTB-Associated Syndromic Thrombocytopenia
- Acute Basophilic Leukemia
- Acute Bilineal Leukemia
- Acute Biphenotypic Leukemia
- Acute Intermittent Porphyria
- Acute Leukemia
- Acute Leukemia Of Ambiguous Lineage
- Acute Lymphoid Leukemia
- Acute Mast Cell Leukemia
- Acute Megakaryoblastic Leukemia
- Acute Megakaryoblastic Leukemia In Adult
- Acute Megakaryoblastic Leukemia In Down Syndrome
- Acute Megakaryoblastic Leukemia Without Down Syndrome
- Acute Monocytic Leukemia
- Acute Myeloblastic Leukemia With Maturation
- Acute Myeloblastic Leukemia Without Maturation
- Acute Myeloid Leukemia
- Acute Myeloid Leukemia And Myelodysplastic Syndromes Related To Alkylating Agent
- Acute Myeloid Leukemia And Myelodysplastic Syndromes Related To Radiation
- Acute Myeloid Leukemia And Myelodysplastic Syndromes Related To Topoisomerase Type 2 Inhibitor
- Acute Myeloid Leukemia By FAB Classification
- Acute Myeloid Leukemia With 11q23 Abnormalities
- Acute Myeloid Leukemia With Abnormal Bone Marrow Eosinophils inv(16)(p13q22) Or t(16;16)(p13;q22)
- Acute Myeloid Leukemia With BCR-ABL1
- Acute Myeloid Leukemia With CBFA2T3-GLIS2 Fusion
- Acute Myeloid Leukemia With CEBPA Somatic Mutations
- Acute Myeloid Leukemia With FUS-ERG Fusion
- Acute Myeloid Leukemia With inv3(p21;q26.2) Or t(3;3)(p21;q26.2)
- Acute Myeloid Leukemia With Minimal Differentiation
- Acute Myeloid Leukemia With MNX1-ETV6 Fusion
- Acute Myeloid Leukemia With Multilineage Dysplasia
- Acute Myeloid Leukemia With Mutated NPM1
- Acute Myeloid Leukemia With NPM1 Somatic Mutations
- Acute Myeloid Leukemia With NPM1-MLF1 Fusion
- Acute Myeloid Leukemia With t(6;9)(p23;q34)
- Acute Myeloid Leukemia With t(8;16)(p11;p13) Translocation
- Acute Myeloid Leukemia With t(8;21)(q22;q22) Translocation
- Acute Myeloid Leukemia With t(9;11)(p22;q23)
- Acute Myeloid Leukemia, Biallelic CEBPA Gene Mutation
- Acute Myeloid Leukemia, CEBPA Gene Mutation
- Acute Myeloid Leukemia, del(13q14-q21)
- Acute Myeloid Leukemia, del(5q31-q32)
- Acute Myeloid Leukemia, der12p
- Acute Myeloid Leukemia, FLT3 Internal Tandem Duplication
- Acute Myeloid Leukemia, FLT3 Tyrosine Kinase Domain Point Mutation
- Acute Myeloid Leukemia, GATA1 Gene Mutation
- Acute Myeloid Leukemia, inv(16)(p13.1;q22)
- Acute Myeloid Leukemia, inv(16)(p13.3;q24.3)
- Acute Myeloid Leukemia, inv(3)(q21.3;q26.2)
- Acute Myeloid Leukemia, KIT Exon 17 Mutation
- Acute Myeloid Leukemia, KIT Exon 8 Mutation
- Acute Myeloid Leukemia, KIT Gene Mutation
- Acute Myeloid Leukemia, KRAS Gene Mutation
- Acute Myeloid Leukemia, Loss Of Chromosome 17p
- Acute Myeloid Leukemia, M6 Type
- Acute Myeloid Leukemia, MLL Gene Rearrangement
- Acute Myeloid Leukemia, Monoallelic CEBPA Gene Mutation
- Acute Myeloid Leukemia, Monosomy 5
- Acute Myeloid Leukemia, Monosomy 7
- Acute Myeloid Leukemia, Non-KMT2A MLLT10 Rearrangement Positive
- Acute Myeloid Leukemia, NRAS Gene Mutation
- Acute Myeloid Leukemia, PTPN11 Gene Mutation
- Acute Myeloid Leukemia, RUNX1 Gene Mutation
- Acute Myeloid Leukemia, t(10;11)(p11.2;q23)
- Acute Myeloid Leukemia, t(10;11)(p12;q23)
- Acute Myeloid Leukemia, t(11;15)(p15;q35)
- Acute Myeloid Leukemia, t(11;17)
- Acute Myeloid Leukemia, t(11;19)(q23.3;p13.3)
- Acute Myeloid Leukemia, t(11;19)(q23;p13)
- Acute Myeloid Leukemia, t(11;19)(q23;p13.1)
- Acute Myeloid Leukemia, t(15;17)(q24;q21)
- Acute Myeloid Leukemia, t(16;16)(p13.1;q22)
- Acute Myeloid Leukemia, t(16;21)(p11;q22)
- Acute Myeloid Leukemia, t(16;21)(q24;q22)
- Acute Myeloid Leukemia, t(1;11)(q21;q23)
- Acute Myeloid Leukemia, t(1;22)
- Acute Myeloid Leukemia, t(1;22)(p13;q13)
- Acute Myeloid Leukemia, t(2;12)
- Acute Myeloid Leukemia, t(3;12)(q23;p12.3)
- Acute Myeloid Leukemia, t(3;3)(q21.3;q26.2)
- Acute Myeloid Leukemia, t(3;5)(q25;q34)
- Acute Myeloid Leukemia, t(4;11)(q21;q23)
- Acute Myeloid Leukemia, t(5;11)(q35;p15)
- Acute Myeloid Leukemia, t(6;11)(q27;q23)
- Acute Myeloid Leukemia, t(6;9)(p23;q34.1)
- Acute Myeloid Leukemia, t(7;12)(q36;p13)
- Acute Myeloid Leukemia, t(8;16)
- Acute Myeloid Leukemia, t(8;21)(q22; q22.1)
- Acute Myeloid Leukemia, t(9;11)(p21.3;q23.3)
- Acute Myeloid Leukemia, t(9;22)(q34.1;q11.2)
- Acute Myeloid Leukemia, t(v;11q23.3)
- Acute Myeloid Leukemia, Trisomy 8
- Acute Myeloid Leukemia, WT1 Gene Mutation
- Acute Myelomonocytic Leukemia M4
- Acute Promyelocytic Leukemia
- Acute Undifferentiated Leukemia
- ADan Amyloidosis
- Adenosine Triphosphatase Deficiency, Anemia Due To
- Adult Acute Lymphoblastic Leukemia
- Adult Acute Monocytic Leukemia
- Adult Lymphoma
- Adult Nodular Lymphocyte Predominant Hodgkin Lymphoma
- Aggressive B-Cell Non-Hodgkin Lymphoma
- Aggressive NK-Cell Leukemia
- AH Amyloidosis
- AIDS-Related Primary Central Nervous System Lymphoma
- AL Amyloidosis
- ALECT2 Amyloidosis
- Aleukemic Leukemia
- Aleukemic Leukemia Cutis
- Aleukemic Monocytic Leukemia Cutis
- ALK-Negative Anaplastic Large Cell Lymphoma
- ALK-Positive Anaplastic Large Cell Lymphoma
- ALK-Positive Large B-Cell Lymphoma
- Alpha-Heavy Chain Disease
- Amyloidosis
- Amyloidosis Cutis Dyschromia
- Amyloidosis, Hereditary Systemic 1
- Amyloidosis, Hereditary Systemic 5
- Amyloidosis, Hereditary Systemic 6
- Amyloidosis, Primary Localized Cutaneous, 1
- Amyloidosis, Primary Localized Cutaneous, 2
- Amyloidosis, Primary Localized Cutaneous, 3
- Anaplastic Large Cell Lymphoma
- Anemia Due To Enzyme Disorder
- Anemia Due To Erythrocyte Enzyme Disorder
- Anemia Of Prematurity
- Anemia, Congenital Dyserythropoietic, Type 1a
- Anemia, Congenital Dyserythropoietic, Type IIIb, Autosomal Recessive
- Anemia, Congenital Dyserythropoietic, Type IVb
- Anemia, Hypochromic Microcytic With Iron Overload
- Anemia, Nonspherocytic Hemolytic, Associated With Abnormality Of Red Cell Membrane
- Anemia, Nonspherocytic Hemolytic, Due To G6PD Deficiency
- Anemia, Nonspherocytic Hemolytic, Possibly Due To Defect In Porphyrin Metabolism
- Anemia, Sideroblastic, 5
- Anemia, Sideroblastic, Pyridoxine-Responsive, Autosomal Recessive
- Angioimmunoblastic T-Cell Lymphoma
- Anus Lymphoma
- Aplastic Anemia
- Appendix Lymphoma
- Aregenerative Anemia
- ATTRV122I Amyloidosis
- ATTRV30M Amyloidosis
- Atypical Chronic Myeloid Leukemia, BCR-ABL1 Negative
- Autoerythrocyte Sensitization Syndrome
- Autoimmune Hemolytic Anemia
- Autoimmune Hemolytic Anemia, Cold Type
- Autoimmune Hemolytic Anemia, Warm Type
- Autoimmune Hemolytic Anemia-Autoimmune Thrombocytopenia-Primary Immunodeficiency Syndrome
- Autoimmune Thrombocytopenia
- Autoimmune Thrombocytopenic Purpura
- Autosomal Dominant Aplasia And Myelodysplasia
- Autosomal Dominant Epidermolytic Ichthyosis
- Autosomal Dominant Macrothrombocytopenia
- Autosomal Dominant Severe Congenital Neutropenia
- Autosomal Dominant Sideroblastic Anemia
- Autosomal Erythropoietic Protoporphyria
- Autosomal Recessive Secondary Polycythemia Not Associated With VHL Gene
- Autosomal Recessive Severe Congenital Neutropenia
- Autosomal Recessive Severe Congenital Neutropenia Due To CSF3R Deficiency
- Autosomal Recessive Severe Congenital Neutropenia Due To CXCR2 Deficiency
- Autosomal Recessive Severe Congenital Neutropenia Due To JAGN1 Deficiency
- Autosomal Recessive Sideroblastic Anemia
B42
- B Acute Lymphoblastic Leukemia With DUX4 Rearrangement
- B Acute Lymphoblastic Leukemia With PAX5 P80R Mutation
- B Lymphoblastic Leukemia Lymphoma With Hyperdiploidy
- B-Cell Acute Lymphoblastic Leukemia
- B-Cell Acute Lymphoblastic Leukemia With t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)
- B-Cell Adult Acute Lymphocytic Leukemia
- B-Cell Childhood Acute Lymphoblastic Leukemia
- B-Cell Chronic Lymphocytic Leukemia
- B-Cell Lymphoma
- B-Cell Lymphoma, Unclassifiable, With Features Intermediate Between Diffuse Large B-Cell Lymphoma And Classical Hodgkin Lymphoma
- B-Cell Non-Hodgkin Lymphoma
- B-Cell Prolymphocytic Leukemia
- B-Lymphoblastic Leukemia With MEF2D Rearrangement
- B-Lymphoblastic Leukemia With MYC Rearrangement
- B-Lymphoblastic Leukemia With NUTM1 Rearrangement
- B-Lymphoblastic Leukemia With PAX5alt
- B-Lymphoblastic Leukemia With TCF3-HLF Fusion
- B-Lymphoblastic Leukemia With ZNF384 Rearrangement
- B-Lymphoblastic Leukemia/lymphoma MLL Rearranged
- B-Lymphoblastic Leukemia/lymphoma With ETV6-RUNX1
- B-Lymphoblastic Leukemia/lymphoma With Hypodiploidy
- B-Lymphoblastic Leukemia/lymphoma With IAMP21
- B-Lymphoblastic Leukemia/lymphoma With IL3-IGH
- B-Lymphoblastic Leukemia/lymphoma With Recurrent Genetic Abnormality
- B-Lymphoblastic Leukemia/lymphoma With t(12;21)(p13.2;q22.1)
- B-Lymphoblastic Leukemia/lymphoma With t(17;19)
- B-Lymphoblastic Leukemia/lymphoma With t(5;14)(q31.1;q32.3)
- B-Lymphoblastic Leukemia/lymphoma With t(7;9)(q11.2;p13.2)
- B-Lymphoblastic Leukemia/lymphoma With t(9;22)(q34.1;q11.2)
- B-Lymphoblastic Leukemia/lymphoma With t(v;11q23.3)
- B-Lymphoblastic Leukemia/lymphoma, BCR-ABL1–like
- Beta-Thalassemia Major
- Beta-Thalassemia-X-Linked Thrombocytopenia Syndrome
- Bladder Lymphoma
- Blast Phase Chronic Myelogenous Leukemia, BCR-ABL1 Positive
- BN2 Diffuse Large B-Cell Lymphoma
- Body Skin Hyperlaxity Due To Vitamin K-Dependent Coagulation Factor Deficiency
- Breast Diffuse Large B-Cell Lymphoma
- Breast Implant-Associated Anaplastic Large Cell Lymphoma
- Breast Lymphoma
- Breast Mucosa-Associated Lymphoid Tissue Lymphoma
- Burkitt Lymphoma
C56
- Cecum Lymphoma
- Central Nervous System Anaplastic Large Cell Lymphoma
- Central Nervous System Leukemia
- Central Nervous System Non-Hodgkin Lymphoma
- Chest Wall Lymphoma
- Child Syndrome
- Childhood Acute Lymphoblastic Leukemia
- Childhood Acute Megakaryoblastic Leukemia
- Childhood Acute Myeloid Leukemia
- Childhood Leukemia
- Childhood Precursor T-Lymphoblastic Lymphoma/leukemia
- Chronic Eosinophilic Leukemia
- Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma
- Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma With Immunoglobulin Heavy Chain Variable-Region Gene Somatic Hypermutation
- Chronic Mast Cell Leukemia
- Chronic Monocytic Leukemia
- Chronic Myelogenous Leukemia, BCR-ABL1 Positive
- Chronic Myelomonocytic Leukemia
- Chronic Neutrophilic Leukemia
- Chuvash Polycythemia
- Classic Hodgkin Lymphoma
- Classic Hodgkin Lymphoma, Lymphocyte-Rich Type
- Coagulation Protein Disease
- Colon Burkitt Lymphoma
- Colon Lymphoma
- Colon Mucosa-Associated Lymphoid Tissue Lymphoma
- Colorectal Diffuse Large B-Cell Lymphoma
- Colorectal Lymphoma
- Combined Immunodeficiency And Megaloblastic Anemia With Or Without Hyperhomocysteinemia
- Combined Immunodeficiency Due To GINS1 Deficiency
- Composite Lymphoma
- Congenital Amegakaryocytic Thrombocytopenia
- Congenital Amegakaryocytic Thrombocytopenia 1
- Congenital Anemia
- Congenital Autosomal Recessive Small-Platelet Thrombocytopenia
- Congenital Dyserythropoietic Anemia
- Congenital Dyserythropoietic Anemia Type 4
- Congenital Dyserythropoietic Anemia Type Type 1B
- Congenital Dyserythropoietic Anemia, Type I
- Congenital Dyserythropoietic Anemia, Type II
- Congenital Dyserythropoietic Anemia, Type III
- Congenital Factor V Deficiency
- Congenital Lethal Erythroderma
- Congenital Nonbullous Ichthyosiform Erythroderma
- Congenital Nonspherocytic Hemolytic Anemia
- Congenital Reticular Ichthyosiform Erythroderma
- Congenital Secondary Polycythemia
- Congenital Sideroblastic Anemia-B-Cell Immunodeficiency-Periodic Fever-Developmental Delay Syndrome
- Constitutional Megaloblastic Anemia With Severe Neurologic Disease
- Constitutional Neutropenia
- Core Binding Factor Acute Myeloid Leukemia
- CPOX-Related Hereditary Coproporphyria
- Cutaneous Nodular Amyloidosis
- Cutaneous Porphyria
- Cyclic Thrombocytopenia
- Cyclical Neutropenia
D35
- Deafness-Lymphedema-Leukemia Syndrome
- Deficiency Anemia
- Dehydration Polycythemia
- Diamond-Blackfan Anemia
- Diamond-Blackfan Anemia 1
- Diamond-Blackfan Anemia 10
- Diamond-Blackfan Anemia 11
- Diamond-Blackfan Anemia 12
- Diamond-Blackfan Anemia 13
- Diamond-Blackfan Anemia 14 With Mandibulofacial Dysostosis
- Diamond-Blackfan Anemia 15 With Mandibulofacial Dysostosis
- Diamond-Blackfan Anemia 16
- Diamond-Blackfan Anemia 17
- Diamond-Blackfan Anemia 18
- Diamond-Blackfan Anemia 19
- Diamond-Blackfan Anemia 2
- Diamond-Blackfan Anemia 20
- Diamond-Blackfan Anemia 21
- Diamond-Blackfan Anemia 22
- Diamond-Blackfan Anemia 3
- Diamond-Blackfan Anemia 4
- Diamond-Blackfan Anemia 5
- Diamond-Blackfan Anemia 6
- Diamond-Blackfan Anemia 7
- Diamond-Blackfan Anemia 8
- Diamond-Blackfan Anemia 9
- DIAPH1-Related Sensorineural Hearing Loss-Thrombocytopenia Syndrome
- Diffuse Large B-Cell Lymphoma Activated B-Cell Type
- Diffuse Large B-Cell Lymphoma Germinal Center B-Cell Type
- Diffuse Large B-Cell Lymphoma Of The Central Nervous System
- Diffuse Large B-Cell Lymphoma With Chronic Inflammation
- Disseminated Intravascular Coagulation
- Disseminated Intravascular Coagulation In Newborn
- Drug-Induced Autoimmune Hemolytic Anemia
- Drug-Induced Methemoglobinemia
E37
- Early T Cell Progenitor Acute Lymphoblastic Leukemia
- EGLN1-Related Erythrocytosis And Pheochromocytoma/paraganglioma Predisposition
- ELANE-Related Neutropenia
- Enteropathy-Associated T-Cell Lymphoma
- Epidermolytic Palmoplantar Keratoderma, 1
- Epstein-Barr Virus-Positive Diffuse Large B-Cell Lymphoma Of The Elderly
- Erythrocyte Galactose Epimerase Deficiency
- Erythrocytosis, Familial, 3
- Erythrocytosis, Familial, 4
- Erythrocytosis, Familial, 5
- Erythrocytosis, Familial, 6
- Erythrocytosis, Familial, 7
- Erythroderma Desquamativum
- Erythroid Neoplasm
- Erythrokeratoderma
- Erythrokeratoderma En Cocardes
- Erythrokeratodermia Variabilis
- Erythrokeratodermia Variabilis Et Progressiva 1
- Erythrokeratodermia Variabilis Et Progressiva 2
- Erythrokeratodermia Variabilis Et Progressiva 3
- Erythrokeratodermia Variabilis Et Progressiva 4
- Erythrokeratodermia Variabilis Et Progressiva 5
- Erythrokeratodermia Variabilis Et Progressiva 6
- Erythrokeratodermia Variabilis Et Progressiva 7
- Erythroleukemia
- Erythroleukemia, Familial, Susceptibility To
- Erythromelalgia
- Erythropoietic Protoporphyria
- Erythropoietic Uroporphyria Associated With Myeloid Malignancy
- Erythropoietin Polycythemia
- Esophagus Lymphoma
- Essential Thrombocythemia
- Evans Syndrome
- Extranodal Nasal NK/T Cell Lymphoma
- Eye Lymphoma
- EZB Diffuse Large B-Cell Lymphoma
- EZB-MYC+ Diffuse Large B-Cell Lymphoma
F34
- Familial Chronic Myelocytic Leukemia-Like Syndrome
- Familial Erythrocytosis
- Familial Hemolytic Anemia
- Familial Hypertryptophanemia
- Familial Porphyria Cutanea Tarda
- Familial Primary Localized Cutaneous Amyloidosis
- Familial Thrombocytosis
- Fanconi Anemia
- Fanconi Anemia Complementation Group A
- Fanconi Anemia Complementation Group B
- Fanconi Anemia Complementation Group C
- Fanconi Anemia Complementation Group D1
- Fanconi Anemia Complementation Group D2
- Fanconi Anemia Complementation Group E
- Fanconi Anemia Complementation Group F
- Fanconi Anemia Complementation Group G
- Fanconi Anemia Complementation Group I
- Fanconi Anemia Complementation Group J
- Fanconi Anemia Complementation Group L
- Fanconi Anemia Complementation Group N
- Fanconi Anemia Complementation Group O
- Fanconi Anemia Complementation Group P
- Fanconi Anemia Complementation Group Q
- Fanconi Anemia Complementation Group R
- Fanconi Anemia Complementation Group T
- Fanconi Anemia Complementation Group U
- Fanconi Anemia Complementation Group V
- Fanconi Anemia, Complementation Group 10
- Fanconi Anemia, Complementation Group S
- Fanconi Anemia, Complementation Group W
- Felty Syndrome
- Fetal And Neonatal Alloimmune Thrombocytopenia
- Follicular Lymphoma
- Follicular Lymphoma, Susceptibility To, 1
G14
- Gallbladder Lymphoma
- Gastric Diffuse Large B-Cell Lymphoma
- Gastric Lymphoma
- Gastric Mantle Cell Lymphoma
- Gastric Mucosa-Associated Lymphoid Tissue Lymphoma
- Gastric Non-Hodgkin Lymphoma
- Gastrointestinal Lymphoma
- GATA Binding Protein 1 Related Thrombocytopenia With Dyserythropoiesis
- Gelatinous Droplike Corneal Dystrophy
- Ghosal Hematodiaphyseal Dysplasia
- Giant Cell Hepatitis With Autoimmune Hemolytic Anemia
- Grade I Lymphomatoid Granulomatosis
- Grade II Lymphomatoid Granulomatosis
- Grade III Lymphomatoid Granulomatosis
H59
- Hairy Cell Leukemia
- Hairy Cell Leukemia Variant
- Harderoporphyria
- Hb SS Disease
- Heart Lymphoma
- Heinz Body Anemia
- Hemoglobin Bart Hydrops Syndrome
- Hemoglobin C Disease
- Hemoglobin C-Beta-Thalassemia Syndrome
- Hemoglobin D Disease
- Hemoglobin E Disease
- Hemoglobin E/beta Thalassemia Disease
- Hemoglobin H Disease
- Hemoglobin Lepore-Beta-Thalassemia Syndrome
- Hemoglobin M Disease
- Hemoglobinopathy Toms River
- Hemolytic Anemia
- Hemolytic Anemia Due To Adenylate Kinase Deficiency
- Hemolytic Anemia Due To Erythrocyte Adenosine Deaminase Overproduction
- Hemolytic Anemia Due To Glucophosphate Isomerase Deficiency
- Hemolytic Anemia Due To Glutathione Reductase Deficiency
- Hemolytic Anemia Due To Hexokinase Deficiency
- Hemolytic Anemia Due To Pyrimidine 5' Nucleotidase Deficiency
- Hemolytic Anemia With Thermal Sensitivity Of Red Cells
- Hemophilia
- Hemophilia A With Vascular Abnormality
- Hemophilia B Leyden
- Heparin-Induced Thrombocytopenia
- Hepatic Cutaneous Porphyria
- Hepatic Porphyria
- Hepatoerythropoietic Porphyria
- Hepatosplenic T-Cell Lymphoma
- Hereditary Amyloidosis
- Hereditary Anemia
- Hereditary Coproporphyria
- Hereditary Factor XI Deficiency Disease
- Hereditary Intrinsic Factor Deficiency
- Hereditary Methemoglobinemia
- Hereditary Persistence Of Fetal Hemoglobin
- Hereditary Persistence Of Fetal Hemoglobin-Beta-Thalassemia Syndrome
- Hereditary Persistence Of Fetal Hemoglobin-Sickle Cell Disease Syndrome
- Hereditary Sideroblastic Anemia
- Hereditary Thrombocytopenia And Hematologic Cancer Predisposition Syndrome
- Hereditary Thrombocytopenia And Hematological Cancer Predisposition Syndrome Associated With RUNX1
- Hereditary Thrombocytosis With Transverse Limb Defect
- Hermansky-Pudlak Syndrome 2
- High Grade B-Cell Lymphoma
- High Grade B-Cell Lymphoma With MYC And/ Or BCL2 And/or BCL6 Rearrangement
- High-Grade B-Cell Lymphoma Double-Hit/triple-Hit
- HMBS-Related Hepatic Porphyria
- Hodgkin Lymphoma, Lymphocyte Depletion
- Hodgkin Lymphoma, Mixed Cellularity
- Hodgkins Lymphoma
- Homocystinuria-Megaloblastic Anemia CblD Type
- Hydroa Vacciniforme-Like Lymphoma
- Hydrops-Lactic Acidosis-Sideroblastic Anemia-Multisystemic Failure Syndrome
- Hypercholanemia, Familial
- Hypercholanemia, Familial 1
- Hypercholanemia, Familial, 2
I19
- Ichthyosis With Erythrokeratoderma
- Idiopathic Aplastic Anemia
- Imerslund-Grasbeck Syndrome
- Immune Deficiency Due To Impaired Neutrophil Phagocytosis And Migration
- Immunoerythromyeloid Hypoplasia
- Indolent B-Cell Non-Hodgkin Lymphoma
- Indolent Primary Cutaneous B-Cell Lymphoma
- Indolent Primary Cutaneous T-Cell Lymphoma
- Infantile Mercury Poisoning
- Inherited Acute Myeloid Leukemia
- Inherited Aplastic Anemia
- Inherited Bleeding Disorder, Platelet-Type
- Inherited Blood Coagulation Disorder
- Inherited Hemoglobinopathy
- Inherited Porphyria
- Inherited Thrombocytopenia
- Intraocular Lymphoma
- Intravascular Large B-Cell Lymphoma
- Iron-Refractory Iron Deficiency Anemia
J1
K3
L31
- Large B-Cell Lymphoma
- Large-Cell Immunoblastic Lymphoma
- Lethal Hemolytic Anemia-Genital Anomalies Syndrome
- Leukemia, Acute Lymphoblastic, Susceptibility To, 3
- Leukemia, Acute Lymphocytic, Susceptibility To, 1
- Leukemia, Acute Lymphocytic, Susceptibility To, 2
- Leukemia, Acute Myeloid, Susceptibility To
- Leukemia, Acute, X-Linked
- Leukemia, Chronic Lymphocytic, Susceptibility To, 1
- Leukemia, Chronic Lymphocytic, Susceptibility To, 2
- Leukemia, Chronic Lymphocytic, Susceptibility To, 3
- Leukemia, Chronic Lymphocytic, Susceptibility To, 4
- Leukemia, Chronic Lymphocytic, Susceptibility To, 5
- Leukemia, Myeloid, Accelerated-Phase
- Leukemia-Lymphoma, Adult T-Cell
- Lichen Amyloidosis
- Liver Diffuse Large B-Cell Lymphoma
- Liver Lymphoma
- Lung Lymphoma
- Lung Non-Hodgkin Lymphoma
- Lymphoblastic Leukemia, Acute, With Lymphomatous Features
- Lymphoblastic Lymphoma
- Lymphoid Leukemia
- Lymphoma, Hodgkin, X-Linked Pseudoautosomal
- Lymphoma, Hodgkin, Y-Linked Pseudoautosomal
- Lymphoma, Non-Hodgkin, Familial
- Lymphoma-Like Variant Infiltrating Bladder Urothelial Carcinoma
- Lymphomatoid Granulomatosis
- Lymphomatoid Papulosis
- Lymphoplasmacytic Lymphoma
- Lymphoplasmacytic Lymphoma Without IgM Production
M53
- Macrocephaly, Neurodevelopmental Delay, Lymphoid Hyperplasia, And Persistent Fetal Hemoglobin
- Macrothrombocytopenia With Mitral Valve Insufficiency
- Macrothrombocytopenia, Isolated
- Macrothrombocytopenia, Isolated, 1, Autosomal Dominant
- Macrothrombocytopenia, Isolated, 2, Autosomal Dominant
- Macrothrombocytopenia-Lymphedema-Developmental Delay-Facial Dysmorphism-Camptodactyly Syndrome
- Macular Amyloidosis
- Majeed Syndrome
- Malignant Lymphoma, Large B-Cell, Diffuse
- Mantle Cell Lymphoma
- Marginal Zone Lymphoma
- Mast Cell Leukemia
- Mast Cell Leukemia With An Associated Myeloid Neoplasm
- Mature T-Cell And NK-Cell Non-Hodgkin Lymphoma
- MCD Diffuse Large B-Cell Lymphoma
- Mediastinal Gray Zone Lymphoma
- Mediastinal Malignant Lymphoma
- Medich Giant Platelet Syndrome
- Megakaryoblastic Acute Myeloid Leukemia With t(1;22)(p13;q13)
- Megaloblastic Anemia, Folate-Responsive
- Megaloblastic Anemia, Thiamine-Responsive, With Diabetes Mellitus And Sensorineural Deafness
- Megaloblastic Anemia-Immunodeficiency Due To Folate Transporter 1 Deficiency
- Methemoglobin Reductase Deficiency
- Methemoglobinemia
- Methemoglobinemia Type 4
- Methemoglobinemia, Alpha Type
- Microcytic Anemia With Liver Iron Overload
- Mild Hemophilia A
- Mild Hemophilia B
- Mixed Phenotype Acute Leukemia
- Mixed Phenotype Acute Leukemia With BCR-ABL1
- Mixed Phenotype Acute Leukemia With MLL Rearranged
- Mixed Phenotype Acute Leukemia With t(9;22)(q34.1;q11.2)
- Mixed Phenotype Acute Leukemia With t(v;11q23.3)
- Mixed Phenotype Acute Leukemia, B/myeloid
- Mixed Phenotype Acute Leukemia,T/myeloid
- Mixed-Type Autoimmune Hemolytic Anemia
- Moderately Severe Hemophilia A
- Moderately Severe Hemophilia B
- Monocytic Leukemia
- Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma
- Monosomy 7 Myelodysplasia And Leukemia Syndrome 1
- Monosomy 7 Myelodysplasia And Leukemia Syndrome 2
- Mucosa-Associated Lymphoma
- Multifocal Lymphangioendotheliomatosis-Thrombocytopenia Syndrome
- Multiple Paragangliomas Associated With Polycythemia
- Myelodysplastic Syndrome With Excess Blasts-1
- Myelodysplastic Syndrome With Excess Blasts-2
- Myelodysplastic Syndrome With Ring Sideroblasts
- Myeloid Leukemia
- Myeloid Leukemia Associated With Down Syndrome
- Myeloid Neoplasm Associated With FGFR1 Rearrangement
- Myelophthisic Anemia
N24
- N1 Diffuse Large B-Cell Lymphoma
- Nasal Cavity Lymphoma
- Neonatal Alloimmune Neutropenia
- Neonatal Autoimmune Hemolytic Anemia
- Neonatal Leukemia
- Neonatal Polycythemia
- Neonatal Thrombocytopenia
- Neurolymphomatosis
- Neutropenia, Lethal Congenital, With Eosinophilia
- Neutropenia, Severe Congenital, 1, Autosomal Dominant
- Neutropenia, Severe Congenital, 10, Autosomal Recessive
- Neutropenia, Severe Congenital, 11, Autosomal Dominant
- Neutropenia, Severe Congenital, 2, Autosomal Dominant
- Neutropenia, Severe Congenital, 8, Autosomal Dominant
- Neutropenia, Severe Congenital, 9, Autosomal Dominant
- Neutropenia-Monocytopenia-Deafness Syndrome
- Nodal Marginal Zone B-Cell Lymphoma
- Nodal T-Follicular Helper Cell Lymphoma, Follicular Type
- Nodular Lymphocyte Predominant Hodgkin Lymphoma
- Nodular Sclerosis Classical Hodgkin Lymphoma
- Non-Autoimmune Hemolytic Anemia
- Nonimmune Chronic Idiopathic Neutropenia Of Adults
- Nonspherocytic Hemolytic Anemia
- Null-Cell Leukemia
O7
P56
- Pancreas Lymphoma
- Pancreatic Insufficiency-Anemia-Hyperostosis Syndrome
- Pancreatic Lymphoma, Familial
- Paranasal Sinus Lymphoma
- Paris-Trousseau Thrombocytopenia
- Paroxysmal Cold Hemoglobinuria
- Paroxysmal Nocturnal Hemoglobinuria
- Paroxysmal Nocturnal Hemoglobinuria 1
- Paroxysmal Nocturnal Hemoglobinuria 2
- Pediatric Lymphoma
- Peripheral T-Cell Lymphoma
- Peripheral T-Cell Lymphoma, Not Otherwise Specified
- Pernicious Anemia
- Philadelphia-Positive Myelogenous Leukemia
- Physiological Polycythemia
- Plasma Cell Leukemia
- Plasmablastic Lymphoma
- Poikiloderma With Neutropenia
- Polycythemia Due To Hypoxia
- Porphyria Cutanea Tarda
- Porphyria, Acute Intermittent, Nonerythroid Variant
- PPOX-Related Hepatic Porphyria
- Precursor B-Cell Acute Lymphoblastic Leukemia
- Precursor Lymphoblastic Lymphoma/leukemia
- Precursor T-Cell Acute Lymphoblastic Leukemia
- Pregerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma
- Primary Bone Lymphoma
- Primary Cutaneous Aggressive Epidermotropic CD8+ T-Cell Lymphoma
- Primary Cutaneous Amyloidosis
- Primary Cutaneous Anaplastic Large Cell Lymphoma
- Primary Cutaneous B-Cell Lymphoma
- Primary Cutaneous CD4+ Small/medium-Sized Pleomorphic T-Cell Lymphoma
- Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type
- Primary Cutaneous Follicle Center Lymphoma
- Primary Cutaneous Gamma-Delta T-Cell Lymphoma
- Primary Cutaneous Gamma/delta-Positive T-Cell Lymphoma
- Primary Cutaneous Lymphoma
- Primary Cutaneous Marginal Zone B-Cell Lymphoma
- Primary Cutaneous T-Cell Lymphoma
- Primary Cutaneous T-Cell Non-Hodgkin Lymphoma
- Primary Effusion Lymphoma
- Primary Erythromelalgia
- Primary Familial Polycythemia Due To EPO Receptor Mutation
- Primary Localized Amyloidosis
- Primary Lymphoma Of The Conjunctiva
- Primary Mediastinal Large B-Cell Lymphoma
- Primary Organ-Specific Lymphoma
- Primary Systemic Amyloidosis
- Primary Thrombocytopenia
- Prolymphocytic Leukemia
- Prostate Lymphoma
- Protein-Deficiency Anemia
- Protoporphyria, Erythropoietic, 1
- Protoporphyria, Erythropoietic, 2
- Pyridoxine Deficiency Anemia
- Pyruvate Kinase Deficiency Of Red Cells
R15
- Radial Aplasia-Thrombocytopenia Syndrome
- Radio-Ulnar Synostosis-Amegakaryocytic Thrombocytopenia Syndrome
- Radioulnar Synostosis With Amegakaryocytic Thrombocytopenia 1
- Radioulnar Synostosis With Amegakaryocytic Thrombocytopenia 2
- Reactive Thrombocytosis
- Rectum Lymphoma
- Recurrent Mast Cell Leukemia
- Refractory Anemia With Excess Blasts In Transformation
- Refractory Cytopenia With Unilineage Dysplasia
- Refractory Hairy Cell Leukemia
- Refractory Precursor T-Lymphoblastic Lymphoma/leukemia
- Relapsed/refractory Diffuse Large B-Cell Lymphoma
- Retina Lymphoma
- Retroperitoneal Lymphoma
- Revesz Syndrome
S42
- Secondary Erythromelalgia
- Secondary Polycythemia
- Severe Congenital Hypochromic Anemia With Ringed Sideroblasts
- Severe Congenital Neutropenia
- Severe Dermatitis-Multiple Allergies-Metabolic Wasting Syndrome
- Severe Hemophilia A
- Severe Hemophilia B
- Sezary Syndrome
- Sickle Cell-Beta-Thalassemia
- Sickle Cell-Hemoglobin C Disease
- Sickle Cell-Hemoglobin D Disease
- Sickle Cell-Hemoglobin E Disease Syndrome
- Sideroblastic Anemia
- Sideroblastic Anemia 2
- Sideroblastic Anemia 3
- Small Cell Variant Anaplastic Large Cell Lymphoma
- Small Intestinal Burkitt Lymphoma
- Small Intestinal Diffuse Large B-Cell Lymphoma
- Small Intestinal Enteropathy-Associated T-Cell Lymphoma
- Small Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma
- Small Intestine Lymphoma
- Spinal Cord Lymphoma
- Splenic Diffuse Large B-Cell Lymphoma
- Splenic Diffuse Red Pulp Small B-Cell Lymphoma
- Splenic Hodgkin Lymphoma
- Splenic Manifestation Of Hairy Cell Leukemia
- Splenic Manifestation Of Leukemia
- Splenic Manifestation Of Prolymphocytic Leukemia
- Splenic Mantle Cell Lymphoma
- Splenic Marginal Zone Lymphoma
- Sporadic Porphyria Cutanea Tarda
- ST2 Diffuse Large B-Cell Lymphoma
- Sternum Lymphoma
- Stormorken Syndrome
- Subacute Leukemia
- Subacute Monocytic Leukemia
- Subcutaneous Panniculitis-Like T-Cell Lymphoma
- Sulfhemoglobinemia
- Sulfhemoglobinemia, Congenital
- Symptomatic Form Of Hemophilia A In Female Carriers
- Symptomatic Form Of Hemophilia B In Female Carriers
- Syndromic Constitutional Thrombocytopenia
T40
- T Lymphoblastic Leukemia/lymphoma
- T-Cell Acute Lymphoblastic Leukemia
- T-Cell Adult Acute Lymphocytic Leukemia
- T-Cell Childhood Acute Lymphocytic Leukemia
- T-Cell Childhood Lymphoblastic Lymphoma
- T-Cell Large Granular Lymphocyte Leukemia
- T-Cell Leukemia
- T-Cell Lymphoma
- T-Cell Prolymphocytic Leukemia
- T-Cell/histiocyte Rich Large B Cell Lymphoma
- T-Lymphoblastic Lymphoma
- Testicular Leukemia
- Testicular Lymphoma
- Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome
- Thrombocytopenia 1
- Thrombocytopenia 10
- Thrombocytopenia 11 With Multiple Congenital Anomalies And Dysmorphic Facies
- Thrombocytopenia 13, Syndromic
- Thrombocytopenia 2
- Thrombocytopenia 3
- Thrombocytopenia 4
- Thrombocytopenia 5
- Thrombocytopenia 6
- Thrombocytopenia 7
- Thrombocytopenia 9
- Thrombocytopenia Due To Immune Destruction
- Thrombocytopenia With Congenital Dyserythropoietic Anemia
- Thrombocytopenia, X-Linked, With Or Without Dyserythropoietic Anemia
- Thrombocytopenic Purpura
- Thrombotic Thrombocytopenic Purpura
- Thymus Lymphoma
- Thyroid Gland Diffuse Large B-Cell Lymphoma
- Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma
- Thyroid Lymphoma
- Tonsillar Lymphoma
- Tracheal Lymphoma
- Transient Erythroblastopenia Of Childhood
- Transient Neonatal Neutropenia
- Transient Neonatal Thrombocytopenia
- Twin Anemia-Polycythemia Sequence