Nystagmus 7, Congenital, Autosomal Dominant (NYS7)

Alias:
Congenital Nystagmus 7
Nys7
Autosomal Dominant Congenital Nystagmus 7
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Nystagmus 7, Congenital, Autosomal Dominant, also known as congenital nystagmus 7, is related to pathologic nystagmus and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Nystagmus 7, Congenital, Autosomal Dominant is NYS7 (Nystagmus 7, Congenital). Affiliated tissues include retina and eye, and related phenotype is horizontal pendular nystagmus.

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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5
26
5

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

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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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