Meningoencephalocele
Symptom Information:
Symptom ID: | HPO:0006888 | ||
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) Cephalocele(HPO:0011815) Encephalocele(HPO:0002084) Meningoencephalocele(HPO:0006888) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the skull(HPO:0000929) Cephalocele(HPO:0011815) Encephalocele(HPO:0002084) Meningoencephalocele(HPO:0006888) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
Meckel syndrome, type 4 | (OMIM:611134) |
Muscle-eye-brain disease | (Orphanet:588) |