Chromosome 19p13.13 Deletion Syndrome

Alias:
Chromosome 19p13.13 Duplication Syndrome
19p13.13 Microdeletion Syndrome
19p13.13 Deletion Syndrome
19p13.13 Microdeletion
Monosomy 19p13.13
Del(19)(p13.13)
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Chromosome 19p13.13 Deletion Syndrome, also known as chromosome 19p13.13 duplication syndrome, is related to strabismus and hypotonia. An important gene associated with Chromosome 19p13.13 Deletion Syndrome is DEL19P13.13 (Chromosome 19p13.13 Deletion Syndrome). Affiliated tissues include eye and brain, and related phenotypes are macrocephaly and abnormal facial shape

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Newborn
<1/1000000
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--
6

Medical Symptom

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

Gene & Mutation

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Gene
Function
Score
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

Title
PMID
Journal
Year
IF
No Data Found!
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