Disease #00673 (Scaphocephaly, maxillary retrusion, and mental retardation, OMIM:609579)
Official abbreviation |
- |
Name |
Scaphocephaly, maxillary retrusion, and mental retardation |
OMIM ID |
609579 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
FGFR2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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