Occipital encephalocele
Symptom Information:
Symptom ID: | HPO:0002085 | ||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) 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) 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) MedDRA: |
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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) |