Meningoencephalocele

Symptom Information:

Symptom ID: HPO:0006888
Synonyms:
Meningoencephalocele (WWS) [OMIM:Meningoencephalocele (WWS)]
Quality:
Cross references:
OMIM: "Meningoencephalocele (WWS)" [OMIM:Meningoencephalocele (WWS)]
UMLS:C0266456 "Meningoencephalocele" [HPO:0006888]
Is a (Direct Parents):
HPO         Encephalocele
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 skull(HPO:0000929)
                   Cephalocele(HPO:0011815)
                      Encephalocele(HPO:0002084)
                         Meningoencephalocele(HPO:0006888)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the skull(HPO:0000929)
                Cephalocele(HPO:0011815)
                   Encephalocele(HPO:0002084)
                      Meningoencephalocele(HPO:0006888)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 (OMIM:236670)
Meckel syndrome, type 4 (OMIM:611134)
Muscle-eye-brain disease (Orphanet:588)