Disease #02235 (GSD9A1 (storage disease, glycogen, type IXa1), OMIM:306000)

Official abbreviation GSD9A1
Name storage disease, glycogen, type IXa1
OMIM ID 306000
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 6
Phenotype entries for this disease 1
Associated with 1 gene PHKA2
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

6 entries on 1 page. Showing entries 1 - 6.
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00222942 - - - M - United Kingdom (Great Britain) - - - - - GSD9A1 - PHKA2 PHKA2 1 1 Shu Yau
00222943 - - - M - United Kingdom (Great Britain) - - - - - GSD9A1 - PHKA2 PHKA2 1 1 Shu Yau
00222944 - - - M - Australia - - - - - GSD9A1 - PHKA2 PHKA2 1 1 Shu Yau
00222945 - - - M - Australia - - - - - GSD9A1 - PHKA2 PHKA2 1 1 Shu Yau
00222946 - - - M - United Kingdom (Great Britain) - - - - - GSD9A1 - PHKA2 PHKA2 1 1 Shu Yau
00464298 R111 - - M no China Chinese - - - - GSD9A1 Weakness of limbs and easy to fall for 1 year, increased creatine kinase. PHKA2 PHKA2 1 1 Xiaomei Luo
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