Spastic Paraplegia 5a, Autosomal Recessive (SPG5A)

Alias:
Spg5a
Hereditary Spastic Paraplegia 5a
Autosomal Recessive Spastic Paraplegia Type 5a
Paraplegia, Spastic, Autosomal Recessive, Type 5a
Autosomal Recessive Spastic Paraplegia 5a
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Spastic Paraplegia 5a, Autosomal Recessive, also known as spg5a, is related to spastic paraplegia type 5a and spastic paraplegia 82, autosomal recessive. An important gene associated with Spastic Paraplegia 5a, Autosomal Recessive is CYP7B1 (Cytochrome P450 Family 7 Subfamily B Member 1). Affiliated tissues include spinal cord and brain, and related phenotypes are spastic paraplegia and impaired vibratory sensation
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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20
121
27

Medical Symptom

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

Gene & Mutation

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No data available

Disease Model

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MGI
Related Gene
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Publications
No data available

References Literature

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