Disease #01798 (GALAC2 (galactokinase deficiency, cataract), OMIM:230200)

Official abbreviation GALAC2
Name galactokinase deficiency, cataract
OMIM ID 230200
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 GALK1
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

2 entries on 1 page. Showing entries 1 - 2.
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00416989 204591 - - M yes Iraq Arabian - - - - GALAC2 Megalencephaly, Leukoencephalopathy, Cataract, Hypergalactosemia, Elevated circulating alkaline phosphatase concentration GALK1 GALK1 1 1 Andreas Laner
00451649 3bINP-089 PubMed: Vela-Amieva 2024 - M no Mexico Mexican - - - - GALAC2 - GALK1 GALK1 2 1 Miriam Erandi Reyna-Fabián
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