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DO Term : brachydactyly type B2 [DOID:0110975] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A brachydactyly characterized by hypoplasia/aplasia of distal phalanges, distal symphalangism, fusion of carpal/tarsal bones, and partial cutaneous syndactyly that has_material_basis_in mutations in the NOG gene on chromosome 17q22.
  • synonyms:
  • 611377,
  • ORDO:140908,
  • BDB2,
  • OMIM:611377,
  • ICD10CM:Q73.8
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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