Disease #04061 (RHDA2 (hypodysplasia/aplasia, renal, type 2 (RHDA-2)), OMIM:615721)

Official abbreviation RHDA2
Name hypodysplasia/aplasia, renal, type 2 (RHDA-2)
OMIM ID 615721
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FGF20
Associated tissues -
Disease features -
Remarks -

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