C1-C2 dislocation

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "C1-C2 dislocation" [OMIM:C1-C2 dislocation]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
Pseudodiastrophic dysplasia (Orphanet:85174)