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Prader-Willi Habitus, Osteopenia, and Camptodactyly

Alias:
Urban-Rogers-Meyer Syndrome
Prader-Willi Habitus-Osteopenia-Camptodactyly Syndrome
Intellectual Disability-Short Stature-Hand Contractures-Genital Anomalies Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Prader-Willi Habitus, Osteopenia, and Camptodactyly, is also known as urban-rogers-meyer syndrome. Related phenotypes are intellectual disability and osteoporosis
Related ID：
MALACARDS：PRD014
OMIM：264010

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Infant
<1/1000000
--
--
2
PRD014

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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