Myelomeningocele

Symptom Information:

Symptom ID: HPO:0002475
Synonyms:
Spina bifida cystica [HPO:0002475]
Myelomeningocele [Orphanet:42180]
Myelocystocele (disorder) [Orphanet:42180]
Meningomyelocele (disorder) [Orphanet:42180]
Myelomeningocele [HPO:0002475]
Meningomyelocele [Orphanet:42180]
Meningomyelocele [OMIM:Meningomyelocele]
Spina bifida cystica [OMIM:Spina bifida cystica]
Meningomyelocele [MedDRA:10027287]
Myelomeningocele [MedDRA:10027287]
Myelomeningocele [OMIM:Myelomeningocele]
Myelomeningocele (less common) [OMIM:Myelomeningocele (less common)]
Myelomeningocele (rare) [OMIM:Myelomeningocele (rare)]
Spina bifida cystica [MedDRA:10071011]
Quality:
Cross references:
Orphanet:42180 "Myelomeningocele" [Orphanet:42180]
OMIM: "Meningomyelocele" [OMIM:Meningomyelocele]
OMIM: "Spina bifida cystica" [OMIM:Spina bifida cystica]
OMIM: "Myelomeningocele" [OMIM:Myelomeningocele]
OMIM: "Myelomeningocele (less common)" [OMIM:Myelomeningocele (less common)]
OMIM: "Myelomeningocele (rare)" [OMIM:Myelomeningocele (rare)]
UMLS:C0025312 "Myelomeningocele" [HPO:0002475]
UMLS:C0025312 "Meningomyelocele" [Orphanet:42180]
Is a (Direct Parents):
MedDRA Congenital and hereditary central nervous system disorders NEC
Orphanet Spinal dysraphism
HPO         Meningocele
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)
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)