juvenile onset Parkinson disease 19A
Parkinson's disease that has material basis in homozygous mutation in the DNAJC6 gene on chromosome 1p31
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juvenile onset Parkinson disease 19A
Summary
juvenile onset Parkinson disease 19A is a rare disease[1].
Key Facts
- juvenile onset Parkinson disease 19A's instance of is recorded as rare disease[2].
- juvenile onset Parkinson disease 19A's instance of is recorded as class of disease[3].
- juvenile onset Parkinson disease 19A is a type of juvenile-onset Parkinson disease[4].
- juvenile onset Parkinson disease 19A is a type of nervous system heredodegenerative disease[5].
- juvenile onset Parkinson disease 19A is a type of genetic disease[6].
- juvenile onset Parkinson disease 19A is a type of autosomal recessive disease[7].
- juvenile onset Parkinson disease 19A is a type of young-onset Parkinson disease[8].
- juvenile onset Parkinson disease 19A's NCI Thesaurus ID is recorded as C198608[9].
- juvenile onset Parkinson disease 19A's health specialty is recorded as neurology[10].
- juvenile onset Parkinson disease 19A's genetic association is recorded as DNAJC6[11].
- juvenile onset Parkinson disease 19A's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060891[12].
- juvenile onset Parkinson disease 19A's exact match is recorded as http://identifiers.org/doid/DOID:0060891[13].
- juvenile onset Parkinson disease 19A's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].