|  Help  |  About  |  Contact Us

DO Term : oculocerebrorenal syndrome [DOID:1056] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndrome that has_material_basis_in mutation in the OCRL gene on chromosome Xq26 and that is characterized by hydrophthalmia, cataract, mental retardation, vitamin D-resistant rickets, amino aciduria, and reduced ammonia production by the kidney.
  • synonyms:
  • MEDDRA:10051707,
  • 309000,
  • GARD:3295,
  • NCI:C84940,
  • ORDO:534,
  • MESH:D009800,
  • Lowe syndrome,
  • SNOMEDCT_US_2023_03_01:79385002,
  • ICD10CM:E72.03,
  • lowe oculocerebrorenal syndrome,
  • OMIM:309000,
  • oculocerebrorenal syndrome of Lowe,
  • UMLS_CUI:C0028860
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