|  Help  |  About  |  Contact Us

DO Term : popliteal pterygium syndrome [DOID:0060055] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndrome characterized by abnormal development of the face, skin and genitals. Clinical expressions of the disease include cleft lip, with or without cleft palate, contractures of the lower extremities, abnormal external genitalia, syndactyly of fingers and/or toes, and a pyramidal skin fold over the hallux nail. It has_material_basis_in mutations in the IRF6 gene on chromosome 1.
  • synonyms:
  • UMLS_CUI:C0265259,
  • OMIM:263650,
  • popliteal web syndrome,
  • 263650,
  • GARD:3242,
  • ORDO:1300,
  • MESH:C562509,
  • OMIM:119500,
  • facio-genito-popliteal syndrome,
  • SNOMEDCT_US_2023_03_01:205820002,
  • ORDO:294963,
  • NCI:C118786,
  • 119500
Quick Links:
 
Quick Links:
 

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