Asymmetric face
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Database Frequency: | 5 / 7739 | ||
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All diseases associated with this symptom:
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES | (OMIM:300887) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Monosomy 22q13 | (Orphanet:48652) |
Phocomelia, Schinzel type | (Orphanet:2879) |
Schilbach-Rott syndrome | (Orphanet:2353) |