Other cytogenic abnormalities have been associated with DGS phenotype including monosomy 10p13, 11p13, and 4q21
Symptom Information:
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Symptom ID:
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OMIM : No Id available
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Synonyms:
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Quality:
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Cross references:
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| OMIM: "Other cytogenic abnormalities have been associated with DGS phenotype including monosomy 10p13, 11p13, and 4q21" [OMIM:Other cytogenic abnormalities have been associated with DGS phenotype including monosomy 10p13, 11p13, and 4q21] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
MedDRA:
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Database Frequency:
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1 / 7739
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Resource:
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All diseases associated with this symptom: