Disease #06115 (SSMG;SRMMD (short stature-micrognathia syndrome), OMIM:617164)
Official abbreviation |
SSMG;SRMMD |
Name |
short stature-micrognathia syndrome |
OMIM ID |
617164 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
ARCN1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
2025-02-28 13:05:45 +01:00 (CET) |
Individuals
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