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DO Term : omodysplasia 1 [DOID:0080844] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  An omodysplasia that is characterized by severe congenital micromelia with shortening and distal tapering of the humeri and femora to give a club-like appearance and that has_material_basis_in homozygous or compound heterozygous mutation in the GPC6 gene on chromosome 13q32.
  • synonyms:
  • 258315,
  • OMIM:258315,
  • MESH:C537746,
  • ORDO:93329,
  • UMLS_CUI:C1850318,
  • SNOMEDCT_US_2023_03_01:725166005
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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