Disease #04655 (MRD29 (mental retardation, autosomal dominant, type 29 (MRD29)), OMIM:616078)
Official abbreviation |
MRD29 |
Name |
mental retardation, autosomal dominant, type 29 (MRD29) |
OMIM ID |
616078 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
6 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
SETBP1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
Date last edited |
2020-11-03 13:29:43 +01:00 (CET) |
Individuals
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