Abnormal gyri

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Abnormal gyri (in 1 of 2 patients) [OMIM:Abnormal gyri (in 1 of 2 patients)]
Quality:
Cross references:
OMIM: "Abnormal gyri" [OMIM:Abnormal gyri]
OMIM: "Abnormal gyri (in 1 of 2 patients)" [OMIM:Abnormal gyri (in 1 of 2 patients)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Congenital brain dysgenesis due to glutamine synthetase deficiency (Orphanet:71278)
Galloway-Mowat syndrome (Orphanet:2065)
Gamma-aminobutyric acid transaminase deficiency (Orphanet:2066)