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DO Term : trichorhinophalangeal syndrome type I [DOID:14743] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndrome that is characterized by short stature, sparse hair, a bulbous nasal tip and cone-shaped epiphyses (the growing ends of bones), as well as severe generalized shortening of all finger and toe bones (brachydactyly).
  • synonyms:
  • Trichorhinophalangeal dysplasia type I,
  • GARD:7802,
  • MESH:C536820,
  • type I trichorhinophalangeal syndrome,
  • trichorhinophalangeal syndrome type 1,
  • UMLS_CUI:C0432233,
  • DOID:0050552,
  • 190350,
  • OMIM:190350,
  • SNOMEDCT_US_2023_03_01:239016009,
  • ORDO:77258,
  • NCI:C75109
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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