neuronal ceroid lipofuscinosis 13
human disease
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neuronal ceroid lipofuscinosis 13
Summary
neuronal ceroid lipofuscinosis 13 is a rare disease[1].
Key Facts
- neuronal ceroid lipofuscinosis 13's instance of is recorded as rare disease[2].
- neuronal ceroid lipofuscinosis 13's instance of is recorded as class of disease[3].
- neuronal ceroid lipofuscinosis 13's subclass of is recorded as neuronal ceroid lipofuscinosis[4].
- neuronal ceroid lipofuscinosis 13's subclass of is recorded as adult neuronal ceroid lipofuscinosis[5].
- neuronal ceroid lipofuscinosis 13's subclass of is recorded as genetic disease[6].
- neuronal ceroid lipofuscinosis 13's OMIM ID is recorded as 615362[7].
- neuronal ceroid lipofuscinosis 13's Disease Ontology ID is recorded as DOID:0110727[8].
- neuronal ceroid lipofuscinosis 13's Orphanet ID is recorded as 352709[9].
- neuronal ceroid lipofuscinosis 13's genetic association is recorded as CTSF[10].
- neuronal ceroid lipofuscinosis 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110727[11].
- neuronal ceroid lipofuscinosis 13's exact match is recorded as http://identifiers.org/doid/DOID:0110727[12].
- neuronal ceroid lipofuscinosis 13's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_352709[13].
- neuronal ceroid lipofuscinosis 13's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79262[14].
- neuronal ceroid lipofuscinosis 13's UMLS CUI is recorded as C3715049[15].
- neuronal ceroid lipofuscinosis 13's ICD-10-CM is recorded as E75.4[16].
- neuronal ceroid lipofuscinosis 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- neuronal ceroid lipofuscinosis 13's Mondo ID is recorded as MONDO_0014147[18].
- neuronal ceroid lipofuscinosis 13's UniProt disease ID is recorded as DI-03853[19].