Search Ontology:

Human Disease

neuronal ceroid lipofuscinosis

Term ID

DOID:14503

Synonyms

hereditary ceroid lipofuscinosis

Definition

References

GARD:10739
ICD10CM:E75.4
MESH:D009472
MIM:PS256730
NCI:C61257
ORDO:216
ORDO:79262
SNOMEDCT_US_2023_03_01:42012007
UMLS_CUI:C0027877

Ontology

Human Disease ( DOID:14503 )

Relationships

is a type of: lipid storage disease

lipid storage disease Show first 5 Terms
has subtype: neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 ... Show All 14 Terms

neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models