Disease #05906 (CHNG7 (hypothyroidism, congenital, nongoitrous, type 7 (CHNG7)), OMIM:618573)

Official abbreviation CHNG7
Name hypothyroidism, congenital, nongoitrous, type 7 (CHNG7)
OMIM ID 618573
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TRHR
Associated tissues -
Disease features -
Remarks -