Chromosome 4q21 Deletion Syndrome

Alias:
4q21 Microdeletion Syndrome
Monosomy 4q21
Chromosome Deletion Syndrome 4q21
Del(4)(q21)
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Chromosome 4q21 Deletion Syndrome, also known as 4q21 microdeletion syndrome, is related to hypotonia and hypertelorism. An important gene associated with Chromosome 4q21 Deletion Syndrome is DEL4Q21 (Chromosome 4q21 Deletion Syndrome). Affiliated tissues include colon, and related phenotypes are hypotonia and global developmental delay

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Newborn
<1/1000000
9
43
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
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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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