You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal recessive infantile hypercalcemia, look for clinical trials, and connect with others living with it — all in one place.
Open the full Autosomal recessive infantile hypercalcemia hub →Autosomal recessive infantile hypercalcemia is a rare condition. Also known as Familial infantile hypercalcemia with suppressed intact parathyroid hormone, IIH, Idiopathic infantile hypercalcemia, Infantile hypercalcaemia type 1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal recessive infantile hypercalcemia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:300547 · OMIM 143880, 616963 · ICD-10 E83.5 · GARD 0017374
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal recessive infantile hypercalcemia, 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 Autosomal recessive infantile hypercalcemia, filtered to your area.
Tomeko shows live, recruiting studies for Autosomal recessive infantile hypercalcemia from ClinicalTrials.gov on the hub.