Meningocele

Symptom Information:

Symptom ID: HPO:0002435
Synonyms:
Congenital meningocele (disorder) [Orphanet:42120]
Meningocele (disorder) [Orphanet:42120]
Congenital meningocele [Orphanet:42120]
Meningocele [Orphanet:42120]
Meningocele [MedDRA:10027266]
Quality:
Cross references:
Orphanet:42120 "Meningocele" [Orphanet:42120]
UMLS:C0025299 "Meningocele" [HPO:0002435]
UMLS:C1261470 "Congenital meningocele" [Orphanet:42120]
UMLS:C0025299 "Meningocele" [Orphanet:42120]
Is a (Direct Parents):
HPO         Abnormality of the meninges
MedDRA Nervous system disorders NEC
HPO         Spina bifida
Orphanet Spinal dysraphism
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)
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)