Disease #01091 (NESCAVS (NESCAV syndrome), OMIM:614255)

Official abbreviation NESCAVS
Name NESCAV syndrome
OMIM ID 614255
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 8
Phenotype entries for this disease 8
Associated with 1 gene KIF1A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00046985 - PubMed: Ohba 2015 - M no Japan Japanese - - - - NESCAVS Cerebellar ataxia, cerebellar atrophy and lower limb spasticity - KIF1A 1 1 Hirotomo Saitsu
00046986 - PubMed: Ohba 2015 - F no Japan Japanese - - - - NESCAVS cerebellar atrophy, lower limb spasticity, and visual disturbance - KIF1A 1 1 Hirotomo Saitsu
00046987 - PubMed: Ohba 2015 - F no Japan Japanese - - - - NESCAVS Developmental delay, cerebellar atrophy, lower limb spasticity, and visual disturbance - KIF1A 1 1 Hirotomo Saitsu
00046988 - PubMed: Ohba 2015 - M no Japan Japanese - - - - NESCAVS Developmental delay, cerebellar atrophy, lower limb spasticity, and visual disturbance - KIF1A 1 1 Hirotomo Saitsu
00046989 - PubMed: Ohba 2015 - F no Japan Japanese - - - - NESCAVS Developmental delay, cerebellar atrophy, lower limb spasticity, and visual disturbance - KIF1A 1 1 Hirotomo Saitsu
00080977 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - NESCAVS Mental retardation, autosomal dominant 9 (OMIM:614255) KIF1A KIF1A 1 1 Daniel Trujillano
00377090 171011 - - F - - - - - - - NESCAVS Congenital blindness, Optic atrophy, Global developmental delay, Umbilical hernia, Microcephaly, Muscular hypotonia KIF1A KIF1A 1 1 Andreas Laner
00448494 286589 - - F no ? (unknown) - - - - - NESCAVS Seizure, Choroid plexus cyst, EEG abnormality, Neonatal epileptic spasm, Myoclonic spasms KIF1A KIF1A 1 1 Andreas Laner
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