All diseases

OMIM ID
218700
OMIM term:
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2; CHNG2
Alternative terms:
THYROID DYSGENESIS
THYROID AGENESIS
THYROID HYPOPLASIA
THYROID, ECTOPIC
HYPOTHYROIDISM, CONGENITAL, DUE TO THYROID DYSGENESIS
HYPOTHYROIDISM, ATHYREOTIC
ATHYREOTIC HYPOTHYROIDISM
RESISTANCE TO THYROTROPIN; RTSH
THYROTROPIN RESISTANCE
(∗) Location:
2q13  
(†) Associated OMIM genes:
PAX8  
(‡) Associated MGI genes:
Foxe1   Pax8  

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