Disease #05908 (CHNG9 (hypothyroidism, congenital, nongoitrous, type 9 (CHNG9)), OMIM:301035)

Official abbreviation CHNG9
Name hypothyroidism, congenital, nongoitrous, type 9 (CHNG9)
OMIM ID 301035
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene IRS4
Associated tissues -
Disease features -
Remarks -