X-Linked Intellectual Disability-Retinitis Pigmentosa Syndrome

Alias:
Aldred Syndrome
Retinitis Pigmentosa and Intellectual Disability Due to Xp11.3 Microdeletion
Retinitis Pigmentosa and Intellectual Disability Due to Monosomy Xp11.3
Retinitis Pigmentosa and Intellectual Disability Due to Del
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
X-Linked Intellectual Disability-Retinitis Pigmentosa Syndrome, also known as aldred syndrome, is related to chromosome xp11.3 deletion syndrome. Affiliated tissues include eye and retina, and related phenotypes are intellectual disability and iris hypopigmentation
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Basic Information

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