Euryblepharon

Symptom Information:

Symptom ID: HPO:0012905
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 12 / 7739
Resource: HPO

All diseases associated with this symptom:

Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Baraitser-Winter syndrome (Orphanet:2995)
Blepharo-cheilo-odontic syndrome (Orphanet:1997)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Caudal appendage - deafness (Orphanet:1123)
Craniosynostosis, Philadelphia type (Orphanet:1527)
Dysmorphism - multiple structural anomalies (Orphanet:1780)
Familial intestinal malrotation - facial anomalies (Orphanet:2454)
Hypertrichosis (Orphanet:79365)
Short stature - heart defect - craniofacial anomalies (Orphanet:1088)