Phenotypes for disease #01091 (NESCAVS (NESCAV syndrome), OMIM:614255)

8 entries on 1 page. Showing entries 1 - 8.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000034353 Cerebellar ataxia, cerebellar atrophy and lower limb spasticity - - Isolated (sporadic) - - 05y - - Hirotomo Saitsu 00046985
0000034354 cerebellar atrophy, lower limb spasticity, and visual disturbance - - Isolated (sporadic) - - 01y - - Hirotomo Saitsu 00046986
0000034355 Developmental delay, cerebellar atrophy, lower limb spasticity, and visual disturbance - - Isolated (sporadic) - - 00y08m - - Hirotomo Saitsu 00046987
0000034356 Developmental delay, cerebellar atrophy, lower limb spasticity, and visual disturbance - - Isolated (sporadic) - - - - - Hirotomo Saitsu 00046988
0000034357 Developmental delay, cerebellar atrophy, lower limb spasticity, and visual disturbance - - Isolated (sporadic) - - 00y10m - - Hirotomo Saitsu 00046989
0000060546 Mental retardation, autosomal dominant 9 (OMIM:614255) - - Isolated (sporadic) - - - - - Daniel Trujillano 00080977
0000272277 Congenital blindness, Optic atrophy, Global developmental delay, Umbilical hernia, Microcephaly, Muscular hypotonia - - Unknown - 02y - - - Andreas Laner 00377090
0000337681 Seizure, Choroid plexus cyst, EEG abnormality, Neonatal epileptic spasm, Myoclonic spasms - - Isolated (sporadic) 00y02m - - - - Andreas Laner 00448494
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