basal laminar drusen
retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium on Bruch membrane and that has material basis in mutations in the CFH gene on chromosome 1q31.3
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basal laminar drusen
Summary
basal laminar drusen is a rare disease[1].
Key Facts
- basal laminar drusen's instance of is recorded as rare disease[2].
- basal laminar drusen's instance of is recorded as class of disease[3].
- basal laminar drusen's subclass of is recorded as drusen[4].
- basal laminar drusen's subclass of is recorded as monogenic disease[5].
- basal laminar drusen's MeSH descriptor ID is recorded as C563034[6].
- basal laminar drusen's OMIM ID is recorded as 126700[7].
- basal laminar drusen's KEGG ID is recorded as H02108[8].
- basal laminar drusen's Disease Ontology ID is recorded as DOID:0060746[9].
- basal laminar drusen's Orphanet ID is recorded as 75376[10].
- basal laminar drusen's genetic association is recorded as CFH[11].
- basal laminar drusen's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060746[12].
- basal laminar drusen's exact match is recorded as http://identifiers.org/doid/DOID:0060746[13].
- basal laminar drusen's UMLS CUI is recorded as C0730295[14].
- basal laminar drusen's ICD-10-CM is recorded as H35.5[15].
- basal laminar drusen's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- basal laminar drusen's Mondo ID is recorded as MONDO_0007472[17].
- basal laminar drusen's UniProt disease ID is recorded as DI-02606[18].