Cerebellofaciodental Syndrome (CFDS)

Alias:
Cerebellar-Facial-Dental Syndrome
Cfds
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cerebellofaciodental Syndrome, also known as cerebellar-facial-dental syndrome, is related to hypomyelinating leukoencephalopathy and leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism. An important gene associated with Cerebellofaciodental Syndrome is BRF1 (BRF1 RNA Polymerase III Transcription Initiation Factor Subunit), and among its related pathways/superpathways are Gene expression (Transcription) and Cytosolic sensors of pathogen-associated DNA. Affiliated tissues include pons and bone, and related phenotypes are scoliosis and global developmental delay
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Antenatal
<1/1000000
11
49
2

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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No data available

Related Drugs

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No data available

Disease Model

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MGI
Related Gene
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Publications
No data available

References Literature

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