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DO Term : congenital hypothyroidism [DOID:0050328] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hypothyroidism that is present at birth.
  • synonyms:
  • DOID:11631,
  • SNOMEDCT_US_2023_03_01:217710005,
  • ICD9CM:243,
  • ICD10CM:E03.1,
  • UMLS_CUI:C0342200,
  • PS275200,
  • UMLS_CUI:C0010308,
  • OMIM:PS275200,
  • NCI:C26734,
  • GARD:1487,
  • MESH:D003409,
  • DOID:11632,
  • ICD10CM:E00.1,
  • NCI:C98921,
  • SNOMEDCT_US_2023_03_01:75065003
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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