Arnold-Chiari type I malformation

Symptom Information:

Symptom ID: HPO:0007099
Synonyms:
Arnold Chiari type I malformation [HPO:0007099]
Chiari I malformation [HPO:0007099]
Arnold Chiari type I malformation [OMIM:Arnold Chiari type I malformation]
Arnold-Chiari type I malformation [OMIM:Arnold-Chiari type I malformation]
Chiari I malformation [OMIM:Chiari I malformation]
Quality:
Cross references:
OMIM: "Arnold Chiari type I malformation" [OMIM:Arnold Chiari type I malformation]
OMIM: "Arnold-Chiari type I malformation" [OMIM:Arnold-Chiari type I malformation]
OMIM: "Chiari I malformation" [OMIM:Chiari I malformation]
Is a (Direct Parents):
HPO         Arnold-Chiari malformation
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
Apert syndrome (Orphanet:87)
Arnold-Chiari malformation type I (Orphanet:268882)
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION (OMIM:601088)
CHROMOSOME 1p32-p31 DELETION SYNDROME (OMIM:613735)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Costello syndrome (Orphanet:3071)
Craniofacial dyssynostosis (Orphanet:1516)
Gordon syndrome (Orphanet:376)
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES (OMIM:609943)
HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM (OMIM:612089)
Lateral meningocele syndrome (Orphanet:2789)
Mowat-Wilson syndrome (Orphanet:2152)
Renal coloboma syndrome (Orphanet:1475)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Syringomyelia (Orphanet:3280)
Williams syndrome (Orphanet:904)