|  Help  |  About  |  Contact Us

DO Term : Schimke immuno-osseous dysplasia [DOID:0060490] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spondyloepiphyseal dysplasia characterized by short stature with hyperpigmented macules, unusual facies, proteinuria with progressive renal failure, lymphopenia with recurrent infections, and cerebral ischaemia. It has_material_basis_in mutations in the SMARCAL1 gene.
  • synonyms:
  • GARD:4984,
  • spondyloepiphyseal dysplasia - nephrotic syndrome,
  • Schimke syndrome,
  • UMLS_CUI:C0877024,
  • Schimke immunoosseous dysplasia,
  • ORDO:1830,
  • 242900,
  • OMIM:242900,
  • NCI:C135087,
  • immunoosseous dysplasia Schimke type,
  • SNOMEDCT_US_2023_03_01:723995003,
  • MESH:C536629
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