Disease #00672 (ABS2 (Antley-Bixler syndrome, without genital anomalies or disordered steroidogenesis (ABS-2)), OMIM:207410)
Official abbreviation |
ABS2 |
Name |
Antley-Bixler syndrome, without genital anomalies or disordered steroidogenesis (ABS-2) |
OMIM ID |
207410 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
FGFR2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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