|
9-amino-2-cyclobutyl-5-(6-methoxy-2-methylpyridin-3-yl)-2,3-dihydro-1H-pyrrolo(3,4-b)quinolin-1-one
|
C575890 |
|
|
Malformations of Cortical Development, Group III
|
D065704 |
[Cortical malformations secondary to abnormal cortical maturation after CELL MIGRATION in NEUROGENESIS. This group includes injury to the cortex during later stages of cortical development such as POLYMICROGYRIA and focal cortical dysplasias.
] |
|
2-((1H-indol-2-yl-methylidene)amino)-5,6,7,8-tetrahydro-4H-cyclohepta(b)thiophene-3-carbonitrile
|
C575880 |
|
|
Hemimegalencephaly
|
D065705 |
[Rare MALFORMATIONS OF CORTICAL DEVELOPMENT, GROUP I characterized by the enlargement of one side of the brain. It is associated with seizures, partial paralysis, and mental retardation.
] |
|
imeglimin
|
C575881 |
|
|
Polymicrogyria
|
D065706 |
[Heterogeneous disorders of cortical malformation characterized by excessive and small fused gyri and shallow sulci of the CORTEX with abnormal cortical lamination. It is considered a malformation secondary to abnormal post-migrational development of the neurons during cerebral cortical development and is associated with EPILEPSY and learning difficulties.
] |
|
mannosylerythritol lipid-D
|
C575882 |
|
|
Schizencephaly
|
D065707 |
[Cortical malformations characterized by grey matter-lined cleft or cyst that extends from the EPENDYMA often to the PIA MATER outer surface. The grey matter that lines the cleft is often POLYMICROGYRIA. It is associated with developmental delay, motor disturbance and seizures.
] |
|
actinotetraose E
|
C575883 |
|
|
Porencephaly
|
D065708 |
[Cortical malformations characterized by white matter-lined cleft or cyst associated with ISCHEMIA and hemorrhagic insults. Symptoms include delayed growth and development, HYPOTONIA; SEIZURES; SPASTIC HEMIPLEGIA and MACROCEPHALY; MICROCEPHALY; or HYDROCEPHALUS. Mutations in the genes encoding COLLAGEN TYPE IV are associated with familial types.
] |
|
prostratol
|
C575884 |
|
|
Common Data Elements
|
D065709 |
[Data elements that are common to multiple data sets across different studies.
] |
|
arcommunol D
|
C575885 |
|
|
Drug Resistance, Multiple, Fungal
|
D026141 |
[The ability of fungi to resist or to become tolerant to several structurally and functionally distinct drugs simultaneously. This resistance phenotype may be attributed to multiple gene mutations.
] |
|
arcommunol E
|
C575886 |
|
|
hopeachinol C
|
C575887 |
|
|
hopeachinol D
|
C575888 |
|
|
Blepharoptosis myopia ectopia lentis
|
C536236 |
|
|
paeciloside A
|
C575889 |
|
|
Blount disease
|
C536237 |
|
