Newfoundland cone-rod dystrophy
cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the RLBP1 gene on chromosome 15q26
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Newfoundland cone-rod dystrophy
Summary
Newfoundland cone-rod dystrophy is a rare disease[1].
Key Facts
- Newfoundland cone-rod dystrophy's instance of is recorded as rare disease[2].
- Newfoundland cone-rod dystrophy's instance of is recorded as class of disease[3].
- Newfoundland cone-rod dystrophy's subclass of is recorded as cone-rod dystrophy[4].
- Newfoundland cone-rod dystrophy's MeSH descriptor ID is recorded as C564391[5].
- Newfoundland cone-rod dystrophy's OMIM ID is recorded as 607476[6].
- Newfoundland cone-rod dystrophy's KEGG ID is recorded as H01009[7].
- Newfoundland cone-rod dystrophy's Disease Ontology ID is recorded as DOID:0111015[8].
- Newfoundland cone-rod dystrophy's genetic association is recorded as RLBP1[9].
- Newfoundland cone-rod dystrophy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111015[10].
- Newfoundland cone-rod dystrophy's exact match is recorded as http://identifiers.org/doid/DOID:0111015[11].
- Newfoundland cone-rod dystrophy's UMLS CUI is recorded as C1843815[12].
- Newfoundland cone-rod dystrophy's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- Newfoundland cone-rod dystrophy's Mondo ID is recorded as MONDO_0011839[14].
- Newfoundland cone-rod dystrophy's UniProt disease ID is recorded as DI-01005[15].