Disease #01996 (HP2 (hyperoxaluria, primary, type II (HP-2)), OMIM:260000)

Official abbreviation HP2
Name hyperoxaluria, primary, type II (HP-2)
OMIM ID 260000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GRHPR
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

1 entry on 1 page. Showing entry 1.
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00411994 201 Abid 2022, submitted - F yes Pakistan Pakistan - - - - HP2 - GRHPR GRHPR 1 1 Aiysha Abid
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