Peculiar facies
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 7 / 7739 | |
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All diseases associated with this symptom:
Aortic arch anomaly - peculiar facies - intellectual deficit | (Orphanet:1110) |
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE | (OMIM:118230) |
EPILEPSY-TELANGIECTASIA | (OMIM:226850) |
Gonadal dysgenesis, XY type - associated anomalies | (Orphanet:1770) |
McDonough syndrome | (Orphanet:2471) |
PEROXISOME BIOGENESIS DISORDER 2B | (OMIM:202370) |
UROFACIAL SYNDROME 1 | (OMIM:236730) |