Porencephaly
Symptom Information:
Symptom ID: | HPO:0002132 | ||||||||
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: Congenital, familial and genetic disorders(MedDRA:10010331) Neurological disorders congenital(MedDRA:10029299) Cerebral disorders congenital(MedDRA:10052634) Porencephaly(HPO:0002132) |
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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) |