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Human Disease and Mouse Model Detail
Human Disease Hypothyroidism, Congenital, Nongoitrous, 2; CHNG2
OMIM ID: 218700
Human Phenotype Ontology associations
Synonyms Athyreotic Hypothyroidism; Hypothyroidism, Athyreotic; Hypothyroidism, Congenital, Due to Thyroid Dysgenesis; Hypothyroidism, Congenital, Nongoitrous; Resistance to Thyrotropin; RTSH; Thyroid Agenesis; Thyroid Dysgenesis; Thyroid Hypoplasia; Thyroid, Ectopic; Thyrotropin Resistance
View all models View ALL (4) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     PAX8* Pax8* View 3 models HomoloGene and HGNC
     FOXE1 Foxe1* View 1 model HomoloGene and HGNC
References Disease References using Mouse Models (5)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory