Pierre Robin Syndrome and Oligodactyly

Alias:
Pierre Robin Sequence-Oligodactyly Syndrome
Robin Sequence-Oligodactyly Syndrome
Robin Sequence and Oligodactyly
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Pierre Robin Syndrome and Oligodactyly, also known as pierre robin sequence-oligodactyly syndrome, is related to isolated pierre robin syndrome and postaxial acrofacial dysostosis. Affiliated tissues include tongue, and related phenotypes are micrognathia and glossoptosis

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Newborn
<1/1000000
--
--
3

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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