Disease #00951 (Scaphocephaly and Axenfeld-Rieger anomaly)
Official abbreviation |
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Name |
Scaphocephaly and Axenfeld-Rieger anomaly |
OMIM ID |
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Inheritance |
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Individuals reported having this disease |
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Phenotype entries for this disease |
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Associated with 1 gene |
FGFR2 |
Associated tissues |
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Disease features |
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Remarks |
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