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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