Posterior fossa cyst

Symptom Information:

Symptom ID: HPO:0007291
Synonyms:
Posterior fossa cyst [OMIM:Posterior fossa cyst]
Posterior fossa cyst (in 1 of 2 patients) [OMIM:Posterior fossa cyst (in 1 of 2 patients)]
Posterior fossa cysts [OMIM:Posterior fossa cysts]
Posterior fossa cysts (WWS) [OMIM:Posterior fossa cysts (WWS)]
Quality:
Cross references:
OMIM: "Posterior fossa cyst" [OMIM:Posterior fossa cyst]
OMIM: "Posterior fossa cyst (in 1 of 2 patients)" [OMIM:Posterior fossa cyst (in 1 of 2 patients)]
OMIM: "Posterior fossa cysts" [OMIM:Posterior fossa cysts]
OMIM: "Posterior fossa cysts (WWS)" [OMIM:Posterior fossa cysts (WWS)]
Is a (Direct Parents):
HPO         Abnormality of the posterior cranial fossa
HPO         Intracranial cystic lesion
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of the skull base(HPO:0002693)
                      Abnormality of the posterior cranial fossa(HPO:0000932)
                         Posterior fossa cyst(HPO:0007291)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the skull(HPO:0000929)
                Abnormality of the skull base(HPO:0002693)
                   Abnormality of the posterior cranial fossa(HPO:0000932)
                      Posterior fossa cyst(HPO:0007291)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
Absent tibia - polydactyly - arachnoid cyst (Orphanet:3328)
Apert syndrome (Orphanet:87)
CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME (OMIM:614195)
Craniosynostosis - Dandy-Walker malformation - hydrocephalus (Orphanet:1538)
Gamma-aminobutyric acid transaminase deficiency (Orphanet:2066)
Isolated Klippel-Feil syndrome (Orphanet:2345)
Joubert syndrome 21 (OMIM:615636)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 (OMIM:236670)
Muscle-eye-brain disease (Orphanet:588)