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DO Term : rapadilino syndrome [DOID:0050774] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndrome that is characterized by radial ray defect, patellae hypoplasia, cleft palate, diarrhea, dislocated joints, limb malformations, long nose and normal intelligence, has_material_basis_in homozygous or compound heterozygous mutation in the DNA helicase gene RECQL4 on chromosome 8q24.
  • synonyms:
  • OMIM:266280,
  • ORDO:3021,
  • UMLS_CUI:C1849453,
  • SNOMEDCT_US_2023_03_01:702413000,
  • GARD:4637,
  • MESH:C535288,
  • 266280
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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents