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Bardet-Biedl Syndrome 21 (BBS21)

Alias:
Bbs21
Bardet-Biedl Syndrome, Type 21
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Bardet-Biedl Syndrome 21, also known as bbs21, is related to cone-rod dystrophy 16 and cone-rod dystrophy 2. An important gene associated with Bardet-Biedl Syndrome 21 is CFAP418 (Cilia And Flagella Associated Protein 418). Affiliated tissues include heart and kidney, and related phenotypes are abnormality of the dentition and delayed speech and language development
Related ID：
MALACARDS：BRD050
OMIM：617406
MESH：D020788

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
1
6
3
BRD050

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
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Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
No Data Found!
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