Meier-Gorlin Syndrome 2 (MGORS2)

Alias:
Mgors2
Meier-Gorlin Syndrome, Type 2
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Meier-Gorlin Syndrome 2, also known as mgors2, is related to x-linked intellectual disability-psychosis-macroorchidism syndrome and hydroxykynureninuria. An important gene associated with Meier-Gorlin Syndrome 2 is ORC4 (Origin Recognition Complex Subunit 4), and among its related pathways/superpathways is Primary ovarian insufficiency. Affiliated tissues include breast and trachea, and related phenotypes are delayed skeletal maturation and microtia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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16
128
4

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
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Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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