Hypothyroidism, congenital, nongoitrous, 1; CHNG1

Disease ID:253
Name:Hypothyroidism, congenital, nongoitrous, 1; CHNG1
Associated with:1 target
Synonyms
Congenital hypothyroidism | Hypothyroidism due to TSH receptor mutations
Database Links
Disease Ontology: DOID:0050328
OMIM: 275200
Orphanet: ORPHA90673

Targets

TSH receptor

Ligands

No ligand related data available for Hypothyroidism, congenital, nongoitrous, 1; CHNG1