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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:Lessel-Kubisch Syndrome
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Accession:DOID:9004277 term browser browse the term
Definition:A disease characterized by short stature and progeroid features, including prematurely gray hair, pinched facies, and scleroderma-like skin changes.
Synonyms:exact_synonym: LSKB
 alt_id: OMIM:618681
For additional species annotation, visit the Alliance of Genome Resources.

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Lessel-Kubisch Syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Mdm2 MDM2 proto-oncogene ISO ClinVar Annotator: match by term: LESSEL-KUBISCH SYNDROME ClinVar
PMID:28846075 NCBI chr 7:60,719,060...60,743,618
Ensembl chr 7:60,719,066...60,743,328
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16092
    Diseases of the Aged 1245
      Premature Aging 67
        Lessel-Kubisch Syndrome 1
Path 2
Term Annotations click to browse term
  disease 16092
    disease of anatomical entity 15341
      musculoskeletal system disease 5736
        connective tissue disease 4135
          bone disease 3505
            bone development disease 1305
              Dwarfism 481
                Lessel-Kubisch Syndrome 1
paths to the root