Genopathy
Gene-Disorder Association · Article
Gene
TFB1M
Transcription Factor B1, Mitochondrial
Disorder
Rare Mitochondrial Non-Syndromic Sensorineural Deafness
First reported 1975
Supporting publications 1
Key publication · disorder Familial hereditary, progressive sensori-neural hearing loss with keratosis palmaris and plantaris.The Journal of laryngology and otology · 1975
Manually curated
Association Review

In brief

The association between TFB1M (Transcription Factor B1, Mitochondrial) and Rare Mitochondrial Non-Syndromic Sensorineural Deafness is a manually-curated gene–disease association, supported by 2 contributing sources, 1 of them expert-curated.

Sources 2
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 1
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

2 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
TFB1M

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Rare Mitochondrial Non-Syndromic Sensorineural Deafness

The disorder

5 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Literature

Reading

1 publication

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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06
Provenance

References & sources

5 references

Every source and publication cited across this dossier, as one numbered reference list.

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