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Osteogenesis Imperfecta, Type X (OI10)

Alias:
Osteogenesis Imperfecta Type 10
Oi10
Osteogenesis Imperfecta Type X
Osteogenesis Imperfecta 10
Oi, Type X
Oi Type X
Oi-X
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Osteogenesis Imperfecta, Type X, also known as osteogenesis imperfecta type 10, is related to brittle bone disorder and bone mineral density quantitative trait locus 3. An important gene associated with Osteogenesis Imperfecta, Type X is SERPINH1 (Serpin Family H Member 1). Affiliated tissues include bone and lung, and related phenotypes are osteopenia and inguinal hernia
Related ID：
MALACARDS：OST127
OMIM：613848
MESH：D010013

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
8
48
2
OST127

Medical Symptom

#
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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