Intellectual Developmental Disorder, Autosomal Dominant 29 (MRD29)

Alias:
Mental Retardation, Autosomal Dominant 29
Mrd29
Autosomal Dominant Intellectual Developmental Disorder 29
Autosomal Dominant Non-Syndromic Intellectual Disability 29
Mental Retardation, Autosomal Dominant, Type 29
Intellectual Disability, Autosomal Dominant 29
Autosomal Dominant Mental Retardation 29
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Intellectual Developmental Disorder, Autosomal Dominant 29, also known as mental retardation, autosomal dominant 29, is related to setbp1 haploinsufficiency disorder and intellectual developmental disorder, autosomal dominant 5. An important gene associated with Intellectual Developmental Disorder, Autosomal Dominant 29 is SETBP1 (SET Binding Protein 1). Affiliated tissues include eye and brain, and related phenotypes are delayed speech and language development and motor delay
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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7
42
10

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

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No data available

Disease Model

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Name
MGI
Related Gene
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Publications
No data available

References Literature

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IF
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