Posterior fossa cyst
Symptom Information:
Symptom ID: | HPO:0007291 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) 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) 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) MedDRA: |
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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) |