Disease #06783 (EPVB6D (Epilepsy, early-onset, vitamin B6-dependent), OMIM:617290)

Official abbreviation EPVB6D
Name Epilepsy, early-onset, vitamin B6-dependent
OMIM ID 617290
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene PROSC
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00464345 - - - - - - - - - - - EPVB6D - ALDH7A1 ALDH7A1 2 1 Min Peng
00464346 - - - - - - - - - - - EPVB6D - ALDH7A1 ALDH7A1 2 1 Min Peng
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