Cerebral hypoplasia
Symptom Information:
Symptom ID: | HPO:0006872 | ||
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
4q21 microdeletion syndrome | (Orphanet:238750) |
Bangstad syndrome | (Orphanet:1227) |
Bifunctional enzyme deficiency | (Orphanet:300) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Meckel syndrome, type 12 | (OMIM:616258) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |