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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:hereditary sensory and autonomic neuropathy type 6
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Accession:DOID:0070151 term browser browse the term
Definition:A hereditary sensory neuropathy characterized by neonatal hypotonia, respiratory and feeding difficulties, impaired psychomotor development, and autonomic abnormalities that has_material_basis_in homozygous mutation in the DST gene on chromosome 6p12. (DO)
Synonyms:exact_synonym: HSAN VI;   HSAN6;   hereditary sensory and autonomic neuropathy, type VI
 primary_id: MIM:614653
 xref: ORDO:314381

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hereditary sensory and autonomic neuropathy type 6 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Dst dystonin ISO ClinVar Annotator: match by term: Hereditary sensory and autonomic neuropathy type 6 | ClinVar Annotator: match by term: Neuropathy, hereditary sensory and autonomic, type VI OMIM
ClinVar		 PMID:9536098 PMID:16199547 PMID:17576681 PMID:20164846 PMID:22113475 More... NCBI chrNW_004936476:4,344,673...4,772,892
Ensembl chrNW_004936476:4,344,716...4,771,878 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14501
    disease of anatomical entity 14165
      nervous system disease 12398
        Nervous System Malformations 2296
          hereditary sensory neuropathy 50
            hereditary sensory and autonomic neuropathy type 6 1
Path 2
Term Annotations click to browse term
  disease 14501
    disease of anatomical entity 14165
      nervous system disease 12398
        central nervous system disease 11098
          neurodegenerative disease 4495
            Nervous System Heredodegenerative Disorders 3086
              hereditary sensory neuropathy 50
                hereditary sensory and autonomic neuropathy type 6 1
paths to the root