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DO Term : XFE progeroid syndrome [DOID:0060590] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A progeroid syndrome that is characterized by aged bird-like facies, lack of subcutaneous fat, dwarfism, cachexia and microcephaly and that has_material_basis_in homozygous mutation in the ERCC4 gene on chromosome 16p13.
  • synonyms:
  • 610965,
  • OMIM:610965,
  • MESH:C567043,
  • XPF-ERCC1 progeroid syndrome,
  • GARD:10628,
  • XFEPS
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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