Disease #01161 (AKV (acrokeratosis verruciformis (AKV, Hopf disease)), OMIM:101900)

Official abbreviation AKV
Name acrokeratosis verruciformis (AKV, Hopf disease)
OMIM ID 101900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 3
Associated with 1 gene ATP2A2
Associated tissues -
Disease features -
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

4 entries on 1 page. Showing entries 1 - 4.
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00055018 - - Family of six generations M - United Kingdom (Great Britain) - - - - - AKV - ATP2A2 ATP2A2 1 1 Michel van Geel
00055073 - - - M - Afghanistan - - - - - AKV - ATP2A2 ATP2A2 1 1 Michel van Geel
00055835 - - Family, 15 affected - - - Druze - - - - AKV - ATP2A2 ATP2A2 1 15 Johan den Dunnen
00056042 - - family, 7 affected ? ? Germany - - - - - AKV - ATP2A2 ATP2A2 1 7 Michel van Geel
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