Disease #01821 (GSD1C (glycogen storage disease, type IC (GSD1C)), OMIM:232240)

Official abbreviation GSD1C
Name glycogen storage disease, type IC (GSD1C)
OMIM ID 232240
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene SLC37A4
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-02-03 14:20:40 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00206446 - - - - - - - - - - - GSD1C - SLC37A4 SLC37A4 1 1 SIB - Livia Famiglietti
00206467 - - - - - - - - - - - GSD1C - SLC37A4 SLC37A4 1 1 SIB - Livia Famiglietti
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