Deletion of chromosome 18p11.2

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Deletion of chromosome 18p11.2" [OMIM:Deletion of chromosome 18p11.2]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Monosomy 18p (Orphanet:1598)