Disease #01593 (RHDA1 (hypodysplasia/aplasia, renal, type 1 (RHDA1)), OMIM:191830)

Official abbreviation RHDA1
Name hypodysplasia/aplasia, renal, type 1 (RHDA1)
OMIM ID 191830
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 ITGA8
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-10-24 17:41:26 +02:00 (CEST)


Individuals

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00095120 - - - F yes - - - - yes - RHDA1 Bilateral renal agenesis - ITGA8 1 1 Karen Stals
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