Disease #02770 (RPIAD (ribose-5-phosphate isomerase deficiency (RPIAD)), OMIM:608611)
Official abbreviation |
RPIAD |
Name |
ribose-5-phosphate isomerase deficiency (RPIAD) |
OMIM ID |
608611 |
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 |
RPIA |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-08-25 17:21:16 +02:00 (CEST) |
Individuals
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