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DO Term : brachydactyly type A1C [DOID:0110977] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A brachydactyly type A1 has_material_basis_in homozygous or heterozygous mutation in the GDF5 gene on chromosome 20q11.
  • synonyms:
  • OMIM:615072,
  • 615072,
  • BDA1C
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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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