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Osteogenesis Imperfecta, Type Xx (OI20)

Alias:
Oi20
Osteogenesis Imperfecta, Type 20
Osteogenesis Imperfecta Type 20
Osteogenesis Imperfecta Type Xx
Osteogenesis Imperfecta 20
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Osteogenesis Imperfecta, Type Xx, also known as oi20, is related to brittle bone disorder and torticollis. An important gene associated with Osteogenesis Imperfecta, Type Xx is MESD (Mesoderm Development LRP Chaperone). Affiliated tissues include bone, and related phenotypes are delayed gross motor development and microcephaly
Related ID：
MALACARDS：OST176
OMIM：618644
MESH：D010013

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
5
28
2
OST176

Medical Symptom

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

Gene & Mutation

#
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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