Translocation or deletions involving 7p13 (severe case reports)

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Translocation or deletions involving 7p13 (severe case reports)" [OMIM:Translocation or deletions involving 7p13 (severe case reports)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Greig cephalopolysyndactyly syndrome (Orphanet:380)