Peculiar facies

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Peculiar facies" [OMIM:Peculiar facies]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 7 / 7739
Resource:

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)