Disease #02680 (NPC2 (Niemann-Pick disease, type C2), OMIM:607625)

Official abbreviation NPC2
Name Niemann-Pick disease, type C2
OMIM ID 607625
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene NPC2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-03-23 09:24:50 +01:00 (CET)


Individuals

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00080909 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - NPC2 Niemann-pick disease, type C2 (OMIM:607625) NPC2 NPC2 1 1 Daniel Trujillano
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