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Metadata
ID	DOID:0111837
Name	congenital nongoitrous hypothyroidism 8
Definition	A congenital hypothyroidism characterized by relatively mild central hypothyroidism that has_material_basis_in heterozygous or hemizygous mutation in the TBL1X gene on chromosome Xp22.3-p22.2. https://www.ncbi.nlm.nih.gov/pubmed/27603907
Xrefs	MIM:301033
Synonyms	CHNG8 [EXACT]
Parent Relationships	is_a congenital hypothyroidism is_a autosomal dominant disease
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance disease has basis in some Abnormality of prenatal development or birth