Cerebral cortical hemiatrophy

Symptom Information:

Symptom ID: HPO:0100308
Synonyms:
Cerebral hemiatrophy [Orphanet:42420]
Cortical atrophy without hydrocephaly/cerebral hemiatrophy/subcortical atrophy [Orphanet:42420]
Subcortical atrophy [Orphanet:42420]
Subcortical atrophy (in some patients) [OMIM:Subcortical atrophy (in some patients)]
Quality:
Cross references:
Orphanet:42420 "Cortical atrophy without hydrocephaly/cerebral hemiatrophy/subcortical atrophy" [Orphanet:42420]
OMIM: "Subcortical atrophy (in some patients)" [OMIM:Subcortical atrophy (in some patients)]
Is a (Direct Parents):
Orphanet Cerebral cortical atrophy
Orphanet Structural anomalies of the nervous system
HPO         Cerebral cortical atrophy
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4 (OMIM:615007)
CADASIL (Orphanet:136)
Huntington disease (Orphanet:399)
MELAS (Orphanet:550)
Mowat-Wilson syndrome (Orphanet:2152)
Wolfram syndrome (Orphanet:3463)