Schizencephaly
Symptom Information:
Symptom ID: | HPO:0010636 | ||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: Nervous system disorders(MedDRA:10029205) Congenital and peripartum neurological conditions(MedDRA:10010335) Congenital and peripartum cerebral disorders(MedDRA:10010334) Schizencephaly(HPO:0010636) |
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Database Frequency: | 5 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Ito hypomelanosis | (Orphanet:435) |
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS | (OMIM:604317) |
Porencephaly | (Orphanet:2940) |
Schizencephaly | (Orphanet:799) |
Vici syndrome | (Orphanet:1493) |