You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness, look for clinical trials, and connect with others living with it — all in one place.
Open the full Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness hub →Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness is a rare condition. Also known as COMMAD syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:603494 · OMIM 617306 · ICD-10 Q87.8 · GARD 0018021
Start by learning the basics from an authoritative source, find a specialist or center that sees Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness, filtered to your area.
Tomeko shows live, recruiting studies for Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness from ClinicalTrials.gov on the hub.