Schizencephaly

Symptom Information:

Symptom ID: HPO:0010636
Synonyms:
Schizencephaly (disorder) [Orphanet:42780]
Schizencephaly [Orphanet:42780]
Schizencephaly [OMIM:Schizencephaly]
Schizencephaly [MedDRA:10073487]
Quality:
Cross references:
Orphanet:42780 "Schizencephaly" [Orphanet:42780]
OMIM: "Schizencephaly" [OMIM:Schizencephaly]
UMLS:C0266484 "Schizencephaly" [HPO:0010636]
UMLS:C0266484 "Schizencephaly" [Orphanet:42780]
Is a (Direct Parents):
Orphanet Structural anomalies of the nervous system
MedDRA Congenital and peripartum cerebral disorders
HPO         Abnormality of the cerebrum
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)
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)