Occipital encephalocele

Symptom Information:

Symptom ID: HPO:0002085
Synonyms:
Occipital meningoencephalocele [HPO:0002085]
Posterior encephalocele [HPO:0002085]
Occipital encephalocele [OMIM:Occipital encephalocele]
Occipital meningoencephalocele [OMIM:Occipital meningoencephalocele]
Posterior encephalocele [OMIM:Posterior encephalocele]
Occipital encephalocele (WWS) [OMIM:Occipital encephalocele (WWS)]
Quality:
Cross references:
OMIM: "Occipital encephalocele" [OMIM:Occipital encephalocele]
OMIM: "Occipital meningoencephalocele" [OMIM:Occipital meningoencephalocele]
OMIM: "Posterior encephalocele" [OMIM:Posterior encephalocele]
OMIM: "Occipital encephalocele (WWS)" [OMIM:Occipital encephalocele (WWS)]
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)
                         Occipital encephalocele(HPO:0002085)
       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)
                      Occipital encephalocele(HPO:0002085)
MedDRA:
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZSYNDROME AND MECKEL SYNDROME (OMIM:213010)
Cobblestone lissencephaly without muscular or ocular involvement (Orphanet:352682)
Goldenhar syndrome (Orphanet:374)
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED (OMIM:241800)
Joubert syndrome 21 (OMIM:615636)
Joubert syndrome 28 (OMIM:617121)
Joubert syndrome with hepatic defect (Orphanet:1454)
Knobloch syndrome (Orphanet:1571)
Lethal occipital encephalocele-skeletal dysplasia syndrome (Orphanet:293925)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 (OMIM:236670)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Meckel syndrome, type 10 (OMIM:614175)
Meckel syndrome, type 11 (OMIM:615397)
Meckel syndrome, type 4 (OMIM:611134)
Meckel syndrome, type 5 (OMIM:611561)
Meckel syndrome, type 6 (OMIM:612284)
Meckel syndrome, type 9 (OMIM:614209)
Muscle-eye-brain disease (Orphanet:588)
VACTERL/VATER association (Orphanet:887)