Porencephaly

Symptom Information:

Symptom ID: HPO:0002132
Synonyms:
Acquired porencephaly (disorder) [Orphanet:42720]
Porencephaly [OMIM:Porencephaly]
Porencephaly [Orphanet:42720]
Porencephaly [MedDRA:10036172]
Porencephalia [MedDRA:10036172]
Porencephalic cyst [MedDRA:10036172]
Porencephalus [MedDRA:10036172]
Porencephalic cyst [OMIM:Porencephalic cyst]
Quality:
Cross references:
Orphanet:42720 "Porencephaly" [Orphanet:42720]
OMIM: "Porencephaly" [OMIM:Porencephaly]
OMIM: "Porencephalic cyst" [OMIM:Porencephalic cyst]
UMLS:C1867983 "Porencephaly" [HPO:0002132]
Is a (Direct Parents):
HPO         Abnormality of the cerebrum
Orphanet Structural anomalies of the nervous system
MedDRA Cerebral disorders congenital
Is a (Whole tree): HPO:
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Neurological disorders congenital(MedDRA:10029299)
       Cerebral disorders congenital(MedDRA:10052634)
          Porencephaly(HPO:0002132)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Adams-Oliver syndrome (Orphanet:974)
Aicardi-Goutières syndrome (Orphanet:51)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Distal 7q11.23 microdeletion syndrome (Orphanet:254351)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Familial vascular leukoencephalopathy (Orphanet:36383)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Linear nevus sebaceus syndrome (Orphanet:2612)
Microgastria - limb reduction defect (Orphanet:2538)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Orofaciodigital syndrome type 4 (Orphanet:2753)
PEHO syndrome (Orphanet:2836)
PORENCEPHALY 2 (OMIM:614483)
Porencephaly (Orphanet:2940)
Porencephaly - cerebellar hypoplasia - internal malformations (Orphanet:2941)
Schizencephaly (Orphanet:799)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)