FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term congenital nongoitrous hypothyroidism 9 ID (Ontology) DOID:0111835 (Human Disease)
Definition A congenital hypothyroidism characterized by a small thyroid gland with low free T4 levels and inappropriately normal levels of thyroid-stimulating hormone that has_material_basis_in hemizygous mutation in the IRS4 gene on chromosome Xq22.3.
Also Known As "CHNG9"
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 Genes
 congenital nongoitrous hypothyroidism 9       1
 for disease ribbon | congenital nongoitrous hypothyroidism 9       1
 model of | congenital nongoitrous hypothyroidism 9       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease__
physical disorder               |
 |__congenital hypothyroidism___|
hypothyroidism                  |
 |__congenital hypothyroidism___|
                                congenital nongoitrous hypothyroidism 9  1 rec.
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Is a congenital hypothyroidism
X-linked recessive disease
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Synonyms
  • "CHNG9" EXACT OMO:0003012
Secondary IDs
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MIM:301035