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Disease Browser
Parent Node:
expandSpinocerebellar Ataxias (D020754)
..Starting node
..expandSpinocerebellar ataxia 25 (C537202)

       Child Nodes:



 Sister Nodes: 
..expandAnemia, sideroblastic spinocerebellar ataxia (C536358)
..expandAtaxia Telangiectasia (D001260) Child6
..expandChorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism (C565850)
..expandGemignani syndrome (C537678)
..expandMachado-Joseph Disease (D017827) Child1
..expandMITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE) (OMIM:271245)
..expandSpastic Ataxia (C564815)
..expandSpastic ataxia Charlevoix-Saguenay type (C536787)
..expandSpinocerebellar Ataxia 10 (C566874)
..expandSpinocerebellar Ataxia 11 (C565772)
..expandSpinocerebellar Ataxia 12 (C565790)
..expandSpinocerebellar Ataxia 15 (C564685)
..expandSpinocerebellar Ataxia 17 (C564616)
..expandSpinocerebellar ataxia 20 (C537199)
..expandSpinocerebellar ataxia 25 (C537202)
..expandSpinocerebellar ataxia 26 (C537203)
..expandSpinocerebellar ataxia 30 (C575214)
..expandSpinocerebellar Ataxia 31 (C566146)
..expandSpinocerebellar Ataxia And Plaque-Like Deposits (C566671)
..expandSpinocerebellar Ataxia with Dysmorphism (C564802)
..expandSpinocerebellar Ataxia with Epilepsy (C564395)
..expandSpinocerebellar Ataxia With Rigidity And Peripheral Neuropathy (C566669)
..expandSpinocerebellar Ataxia, Autosomal Recessive 7 (C563753)
..expandSpinocerebellar Ataxia, Autosomal Recessive 8 (C565188)
..expandSpinocerebellar Ataxia, Autosomal Recessive 9 (C567436)
..expandSpinocerebellar Ataxia, X-Linked 1 (C563134)
..expandSpinocerebellar Ataxia, X-Linked 5 (C567478)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:10504
Name:Spinocerebellar ataxia 25
Definition:
Alternative IDs:OMIM:608703
ParentIDs:MESH:D020754
TreeNumbers:C10.228.140.252.190.530/C537202 |C10.228.140.252.700.700/C537202 |C10.228.854.787.875/C537202 |C10.574.500.825.700/C537202 |C10.597.350.090.500.530/C537202 |C16.320.400.780.875/C537202
Synonyms:SCA25 |Spinocerebellar ataxia type 25
Slim Mappings:Genetic disease (inborn)|Nervous system disease
Reference: MedGen: C537202
MeSH: C537202
OMIM: 608703;

Genes: SCA25;
Phenotypes
1 HP:0000006Autosomal dominant inheritance
2 HP:0006944Abolished vibration sense
3 HP:0002522Areflexia of lower limbs
4 HP:0001251Ataxia
5 HP:0003487Babinski sign
6 HP:0001272Cerebellar atrophy
7 HP:0003380Decreased number of peripheral myelinated nerve fibers
8 HP:0001260Dysarthria
9 HP:0000317Facial myokymia
10 HP:0011468Facial tics
11 HP:0007328Impaired pain sensation
12 HP:0000639Nystagmus
13 HP:0001761Pes cavus
14 HP:0007663Reduced visual acuity
15 HP:0002650Scoliosis
16 HP:0000763Sensory neuropathy
17 HP:0000486Strabismus
18 HP:0000012Urinary urgency
19 HP:0000505Visual impairment
20 HP:0002013Vomiting
Disease Causing ClinVar Variants