Disease #01859 (HYRPRO2 (Hyperprolinemia, type II), OMIM:239510)

Official abbreviation HYRPRO2
Name Hyperprolinemia, type II
OMIM ID 239510
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene ALDH4A1
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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00180247 - - - - - - - - - - - HYRPRO2 - ALDH4A1 ALDH4A1 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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