Disease #04177 (OMCS (Oliver-McFarlane syndrome (OMCS)), OMIM:275400)
Official abbreviation |
OMCS |
Name |
Oliver-McFarlane syndrome (OMCS) |
OMIM ID |
275400 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
4 |
Phenotype entries for this disease |
4 |
Associated with 1 gene |
PNPLA6 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-01-27 14:10:39 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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