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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Schimke immuno-osseous dysplasia
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Accession:DOID:0060490 term browser browse the term
Definition: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. (DO)
Synonyms:exact_synonym: SIOD;   Schimke immunoosseous dysplasia;   Schimke syndrome;   immunoosseous dysplasia Schimke type;   spondyloepiphyseal dysplasia - nephrotic syndrome
 primary_id: MESH:C536629
 alt_id: OMIM:242900;   RDO:0002264
 xref: GARD:4984;   NCI:C135087;   ORDO:1830
For additional species annotation, visit the Alliance of Genome Resources.

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Schimke immuno-osseous dysplasia term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Smarcal1 Swi/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 ISO DNA:mutations:multiple (human)
ClinVar Annotator: match by OMIM:242900
CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: Schimke immunoosseous dysplasia
ClinVar Annotator: match by term: Schimke immuno-osseous dysplasia
PMID:9536098 PMID:11799392 PMID:15523612 PMID:15880370 PMID:16237566 PMID:16840568 PMID:17089404 PMID:17576681 PMID:18805831 PMID:18974355 PMID:19127206 PMID:19793864 PMID:20301550 PMID:21914180 PMID:22998683 PMID:23671665 PMID:24589093 PMID:25741868 PMID:25748404 PMID:26089390 PMID:26195148 PMID:26499378 PMID:28492532 PMID:28780565 PMID:28796785 PMID:28844315 PMID:29802247 PMID:30026777 PMID:30784191, PMID:11799392 RGD:1599053 NCBI chr 9:79,943,775...79,990,230
Ensembl chr 9:79,944,132...79,990,229
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16929
    syndrome 7653
      nephrotic syndrome 133
        Schimke immuno-osseous dysplasia 1
Path 2
Term Annotations click to browse term
  disease 16929
    disease of anatomical entity 16296
      Urogenital Diseases 4204
        urinary system disease 2108
          kidney disease 1887
            proteinuria 531
              nephrosis 253
                nephrotic syndrome 133
                  Schimke immuno-osseous dysplasia 1
paths to the root