Myelomeningocele
Symptom Information:
Symptom ID: | HPO:0002475 | ||||||||||||||
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 vertebral column(HPO:0000925) Spinal dysraphism(HPO:0010301) Spina bifida(HPO:0002414) Meningocele(HPO:0002435) Myelomeningocele(HPO:0002475) MedDRA: Nervous system disorders(MedDRA:10029205) Congenital and peripartum neurological conditions(MedDRA:10010335) Congenital and hereditary central nervous system disorders NEC(MedDRA:10010332) Myelomeningocele(HPO:0002475) |
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Database Frequency: | 29 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
CHILD syndrome | (Orphanet:139) |
Caudal duplication | (Orphanet:1756) |
Cerebro-costo-mandibular syndrome | (Orphanet:1393) |
Cloacal exstrophy | (Orphanet:93929) |
Diaphanospondylodysostosis | (Orphanet:66637) |
Ectrodactyly - spina bifida - cardiopathy | (Orphanet:1894) |
Embryofetopathy due to oral anticoagulant therapy | (Orphanet:1914) |
Exstrophy-epispadias complex | (Orphanet:322) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fraser syndrome | (Orphanet:2052) |
Frontal encephalocele | (Orphanet:1931) |
Hemihypertrophy | (Orphanet:2128) |
Iniencephaly | (Orphanet:63259) |
Isolated spina bifida | (Orphanet:823) |
Kousseff syndrome | (Orphanet:2351) |
Lathosterolosis | (Orphanet:46059) |
Limb body wall complex | (Orphanet:2369) |
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO | (OMIM:182940) |
Neural tube closure defect | (Orphanet:268357) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
PELVIS syndrome | (Orphanet:83628) |
PHAVER syndrome | (Orphanet:2876) |
SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE | (OMIM:613686) |
Sacrococcygeal dysgenesis association | (Orphanet:1773) |
Split hand - urinary anomalies - spina bifida | (Orphanet:2437) |
Trisomy 8q | (Orphanet:1752) |
Waardenburg syndrome | (Orphanet:3440) |
Waardenburg syndrome type 1 | (Orphanet:894) |