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Metaphyseal Dysplasia-Maxillary Hypoplasia-Brachydacty Syndrome

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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Metaphyseal Dysplasia-Maxillary Hypoplasia-Brachydacty Syndrome is related to metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly and brachydactyly. An important gene associated with Metaphyseal Dysplasia-Maxillary Hypoplasia-Brachydacty Syndrome is RUNX2 (RUNX Family Transcription Factor 2). Affiliated tissues include bone.
Related ID：
MALACARDS：MTP030

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Unknown
<1/1000000
1
20
2
MTP030

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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