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
|