Cerebral hypoplasia

Symptom Information:

Symptom ID: HPO:0006872
Synonyms:
Cerebral hypoplasia [OMIM:Cerebral hypoplasia]
Quality:
Cross references:
OMIM: "Cerebral hypoplasia" [OMIM:Cerebral hypoplasia]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the cerebrum
Is a (Whole tree): HPO:
MedDRA:
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)