Disease #00087 (MALNS;SOTOS2 (Malan syndrome (previously SOTOS2)), OMIM:614753)
Official abbreviation |
MALNS;SOTOS2 |
Name |
Malan syndrome (previously SOTOS2) |
OMIM ID |
614753 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
60 |
Phenotype entries for this disease |
4 |
Associated with 1 gene |
NFIX |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2012-11-19 10:06:43 +01:00 (CET) |
Date last edited |
2023-06-28 09:24:49 +02:00 (CEST) |
Individuals
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