Osteogenesis Imperfecta, Type Xvii (OI17)

Alias:
Osteogenesis Imperfecta Type 17
Oi17
Osteogenesis Imperfecta Type Xvii
Osteogenesis Imperfecta 17
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Osteogenesis Imperfecta, Type Xvii, also known as osteogenesis imperfecta type 17, is related to osteoporosis, juvenile and osteogenesis imperfecta, type vi. An important gene associated with Osteogenesis Imperfecta, Type Xvii is SPARC (Secreted Protein Acidic And Cysteine Rich). Affiliated tissues include bone and skin, and related phenotypes are reduced bone mineral density and osteoporosis
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
5
36
1

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!
Wechat
Comparison
Al agent
Tutorials
Back to top