Chiari type I malformation

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Chiari type I malformation (in some patients) [OMIM:Chiari type I malformation (in some patients)]
Quality:
Cross references:
OMIM: "Chiari type I malformation" [OMIM:Chiari type I malformation]
OMIM: "Chiari type I malformation (in some patients)" [OMIM:Chiari type I malformation (in some patients)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
Familial lambdoid synostosis (Orphanet:3267)