Disease #01149 (OPSMD (opsismodysplasia (OPSMD)), OMIM:258480)
| Official abbreviation |
OPSMD |
| Name |
opsismodysplasia (OPSMD) |
| OMIM ID |
258480 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
INPPL1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-09-29 15:46:56 +02:00 (CEST) |
Individuals
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