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DO Term : distal arthrogryposis type 1 [DOID:0111596] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A distal arthrogryposis characterized by autosomal domiant inheritance of contractures of the distal regions of the hands and feet with no facial involvement or other anomalies.
  • synonyms:
  • MESH:C565097,
  • digitotalar dysmorphism,
  • 126050,
  • ORDO:1146,
  • OMIM:126050,
  • GARD:787,
  • DA1,
  • SNOMEDCT_US_2021_09_01:715314008
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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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