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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