Occipital meningocele
Symptom Information:
Symptom ID: | HPO:0002436 | ||
Synonyms: |
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Quality: | |||
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 the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal axial skeleton morphology(HPO:0009121) Abnormality of the vertebral column(HPO:0000925) Spinal dysraphism(HPO:0010301) Spina bifida(HPO:0002414) Meningocele(HPO:0002435) Occipital meningocele(HPO:0002436) MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ARIMA SYNDROME | (OMIM:243910) |
Joubert syndrome 1 | (OMIM:213300) |
Joubert syndrome with oculorenal defect | (Orphanet:2318) |
Phocomelia, Schinzel type | (Orphanet:2879) |