Meningocele
Symptom Information:
Symptom ID: | HPO:0002435 | ||||||||
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 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) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Nervous system disorders NEC(MedDRA:10057185) Meningocele(HPO:0002435) |
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Database Frequency: | 23 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Acromelic frontonasal dysplasia | (Orphanet:1827) |
Aminopterin/methotrexate embryofetopathy | (Orphanet:1908) |
Autosomal recessive spondylocostal dysostosis | (Orphanet:2311) |
CHILD syndrome | (Orphanet:139) |
Cerebro-costo-mandibular syndrome | (Orphanet:1393) |
Cleft lip/palate - deafness - sacral lipoma | (Orphanet:2003) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Hepatic fibrosis - renal cysts - intellectual deficit | (Orphanet:2031) |
Humero-radial synostosis | (Orphanet:3265) |
Isolated spina bifida | (Orphanet:823) |
Lateral meningocele syndrome | (Orphanet:2789) |
Lathosterolosis | (Orphanet:46059) |
Marfan syndrome | (Orphanet:558) |
Meckel syndrome, type 2 | (OMIM:603194) |
Muscle-eye-brain disease | (Orphanet:588) |
Neurocutaneous melanocytosis | (Orphanet:2481) |
PAGOD syndrome | (Orphanet:991) |
Phocomelia, Schinzel type | (Orphanet:2879) |
Thoraco-abdominal enteric duplication | (Orphanet:1759) |
Triploidy | (Orphanet:3376) |
Von Voss-Cherstvoy syndrome | (Orphanet:3439) |
Waardenburg syndrome type 1 | (Orphanet:894) |
Wildervanck syndrome | (Orphanet:3456) |