Spastic Cerebral Palsy

Alias:
Hemiplegic Infantile Cerebral Palsy
Postnatal Infantile Hemiplegia Nos
Spastic Hemiplegic Cerebral Palsy
Congenital Spastic Hemiplegia
Hemiplegic Cerebral Palsy
Congenital Hemiplegia Nos
Palsy, Cerebral, Spastic
Infantile Hemiplegia Nos
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Spastic Cerebral Palsy, also known as hemiplegic infantile cerebral palsy, is related to spastic paraplegia 2, x-linked and spastic diplegia. An important gene associated with Spastic Cerebral Palsy is FBXO31 (F-Box Protein 31), and among its related pathways/superpathways is Vesicle-mediated transport. The drugs Acetylcholine and incobotulinumtoxinA have been mentioned in the context of this disorder. Affiliated tissues include cortex and brain, and related phenotypes are nervous system and homeostasis/metabolism
Related ID:
ICD11:1426032265

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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30
212
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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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
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IF
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