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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:Griscelli syndrome type 1
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Accession:DOID:0060832 term browser browse the term
Definition:A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and neurological impairment without immunodeficiency that has_material_basis_in mutations in the MYO5A gene on chromosome 15q21.2. (DO)
Synonyms:exact_synonym: GS1;   Griscelli syndrome with neurologic impairment;   Griscelli syndrome with neurological impairment;   Griscelli syndrome, cutaneous and neurologic type;   Griscelli syndrome, cutaneous and neurological type;   Griscelli-Prunieras syndrome type 1;   Griscelli-Pruniéras syndrome type 1;   MYO5A-RELATED CONDITION;   Partial albinism and primary neurologic disease without hemophagocytic syndrome;   hypopigmentation-neurologic impairment syndrome
 xref: GARD:2566;   MESH:C537301;   MIM:214450;   MONDO:0008962;   ORDO:79476



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Griscelli syndrome type 1 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G MYO5A myosin VA ISO ClinVar Annotator: match by term: Griscelli syndrome type 1 | ClinVar Annotator: match by term: MYO5A-related condition OMIM
ClinVar
PMID:9207796 PMID:9536098 PMID:10704277 PMID:12058346 PMID:17576681 More... NCBI chr15:31,246,192...31,470,040
Ensembl chr15:49,578,491...49,704,319
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15835
    syndrome 10731
      primary immunodeficiency disease 4140
        Griscelli syndrome 7
          Griscelli syndrome type 1 1
Path 2
Term Annotations click to browse term
  disease 15835
    Pathological Conditions, Signs and Symptoms 12339
      Signs and Symptoms 10388
        Neurologic Manifestations 10069
          sensory system disease 7070
            Otorhinolaryngologic Diseases 1737
              auditory system disease 1013
                Hearing Disorders 796
                  Hearing Loss 790
                    sensorineural hearing loss 599
                      Griscelli syndrome 7
                        Griscelli syndrome type 1 1
paths to the root