Phenotypes for disease #01798 (GALAC2 (galactokinase deficiency, cataract), OMIM:230200)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000308500 Megalencephaly, Leukoencephalopathy, Cataract, Hypergalactosemia, Elevated circulating alkaline phosphatase concentration - - Familial, autosomal recessive 00y06m - - - - Andreas Laner 00416989
0000340310 - Galactosemia Galactokinase deficiency with cataracts Familial, autosomal recessive - 00y01m - - - Miriam Erandi Reyna-Fabián 00451649
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