Spastic Paraplegia 19, Autosomal Dominant (SPG19)

Alias:
Spg19
Autosomal Dominant Spastic Paraplegia Type 19
Hereditary Spastic Paraplegia 19
Autosomal Dominant Spastic Paraplegia 19
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Spastic Paraplegia 19, Autosomal Dominant, also known as spg19, is related to spasticity and spastic paraplegia 20, autosomal recessive, and has symptoms including urgency of micturition and abnormal pyramidal signs. An important gene associated with Spastic Paraplegia 19, Autosomal Dominant is SPG19 (Spastic Paraplegia 19 (Autosomal Dominant)). Affiliated tissues include spinal cord, and related phenotypes are hyperreflexia and babinski sign

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
<1/1000000
9
55
1

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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