Occipital myelomeningocele

Symptom Information:

Symptom ID: HPO:0007271
Synonyms:
Occipital myelomeningocele (less common) [OMIM:Occipital myelomeningocele (less common)]
Quality:
Cross references:
OMIM: "Occipital myelomeningocele (less common)" [OMIM:Occipital myelomeningocele (less common)]
Is a (Direct Parents):
HPO         Occipital 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)
                            Occipital meningocele(HPO:0002436)
                               Occipital myelomeningocele(HPO:0007271)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Joubert syndrome (Orphanet:475)
Joubert syndrome 1 (OMIM:213300)