Craniofacial anomalies

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Craniofacial anomalies" [OMIM:Craniofacial anomalies]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Beckwith-Wiedemann syndrome due to CDKN1C mutation (Orphanet:231120)
FRASER-LIKE SYNDROME (OMIM:229230)