Disease #02733 (ARPHM;PVNH2 (heterotopia, periventricular, autosomal recessive (ARPHM, periventricular heterotopia type 2 (PVNH-2))), OMIM:608097)

Official abbreviation ARPHM;PVNH2
Name heterotopia, periventricular, autosomal recessive (ARPHM, periventricular heterotopia type 2 (PVNH-2))
OMIM ID 608097
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 ARFGEF2
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00032830 - Michaelides et al., Submitted - - - United Kingdom (Great Britain) British - - - - ARPHM;PVNH2 - PROM1 PROM1 1 3 Pascal Escher
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