Disease #00086 (MRSHSS (Marshall-Smith syndrome (MRSHSS)), OMIM:602535)
| Official abbreviation |
MRSHSS |
| Name |
Marshall-Smith syndrome (MRSHSS) |
| OMIM ID |
602535 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
18 |
| Phenotype entries for this disease |
18 |
| Associated with 1 gene |
NFIX |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-11-19 10:06:06 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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