Disease #05471 (PVNH7 (heterotopia, nodular, periventricular, type 7), OMIM:617201)

Official abbreviation PVNH7
Name heterotopia, nodular, periventricular, type 7
OMIM ID 617201
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene NEDD4L
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2018-08-24 17:08:46 +02:00 (CEST)
Date last edited 2024-04-19 19:00:58 +02:00 (CEST)


Individuals

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00228934 Fam44 PubMed: Pissard 2006 - - - France - - - - - favism, PVNH7 - PKLR PKLR 1 1 Richard van Wijk
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