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 is a type of neuronal ceroid lipofuscinosis[4].
- neuronal ceroid lipofuscinosis 13 is a type of adult neuronal ceroid lipofuscinosis[5].
- neuronal ceroid lipofuscinosis 13 is a type of genetic disease[6].
- neuronal ceroid lipofuscinosis 13's genetic association is recorded as CTSF[7].
- neuronal ceroid lipofuscinosis 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110727[8].
- neuronal ceroid lipofuscinosis 13's exact match is recorded as http://identifiers.org/doid/DOID:0110727[9].
- neuronal ceroid lipofuscinosis 13's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_352709[10].
- neuronal ceroid lipofuscinosis 13's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79262[11].
- neuronal ceroid lipofuscinosis 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].