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Foxg1 Syndrome Due to 14q12 Microdeletion

Alias:
Monosomy 14q12
Del(14)(q12)
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Foxg1 Syndrome Due to 14q12 Microdeletion, also known as monosomy 14q12, is related to hypertelorism and microcephaly. An important gene associated with Foxg1 Syndrome Due to 14q12 Microdeletion is FOXG1 (Forkhead Box G1). Related phenotypes are hypotonia and developmental regression
Related ID：
MALACARDS：FXG002

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Newborn
<1/1000000
1
10
--
FXG002

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

Name
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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