Disease #01174 (PLCA1 (amyloidosis, primary localized cutaneous, type 1 (PLCA1), OMIM:105250)

Official abbreviation PLCA1
Name amyloidosis, primary localized cutaneous, type 1 (PLCA1
OMIM ID 105250
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene OSMR
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

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00092262 - PubMed: Tarailo-Graovac 2016, Journal: Tarailo-Graovac 2016 - - - United States - - - - - PLCA1, VRJS facial dysmorphism, short stature (Verheij syndrome), mild IDD ,severe early onset eczema (amyloidosis, primary localized cutaneous, recessive) OSMR, PUF60 - - 1 Johan den Dunnen
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