Abnormality of the posterior cranial fossa
Symptom Information:
Symptom ID: | HPO:0000932 | ||||||
Synonyms: |
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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 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) 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) MedDRA: |
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Database Frequency: | 5 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Intellectual deficit, X-linked, Kroes type | (Orphanet:163961) |
Isotretinoin-like syndrome | (Orphanet:2306) |
Meckel syndrome, type 9 | (OMIM:614209) |
Moebius syndrome | (Orphanet:570) |