Disease #04158 (alpha-actinin-3 deficiency, OMIM:102574)

Official abbreviation -
Name alpha-actinin-3 deficiency
OMIM ID 102574
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene ACTN3
Associated tissues -
Disease features -
Remarks -
Date created 2014-12-13 11:02:38 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00025500 - PubMed: North 1999 3-generation family, 5 homozygous individuals - - Australia - - - - - alpha-actinin-3 deficiency 2/5 individuals with congenital muscular dystrophy ACTN3 ACTN3 1 5 Johan den Dunnen
00025501 - PubMed: North 1999 125 individuals with DNA and muscle biopsy - - Australia - - - - - alpha-actinin-3 deficiency ACTN3 staining muscle negative ACTN3 ACTN3 1 48 Johan den Dunnen
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