Disease #01997 (OPLAHD (5-oxoprolinase deficiency (OPLAHD)), OMIM:260005)

Official abbreviation OPLAHD
Name 5-oxoprolinase deficiency (OPLAHD)
OMIM ID 260005
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene OPLAH
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

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00458570 - - - F - - (not applicable) white - - - - OPLAHD HP:0040142 - OPLAH 2 1 Marketa Wayhelova
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