Genopathy
Gene-Disorder Association · Article
Gene
NR0B1
Nuclear Receptor Subfamily 0 Group B Member 1
Disorder
Kallmann Syndrome
First reported 1996
Supporting publications 1
Key publication · gene–disorder Inherited disorders of the gonadotropin hormones.Molecular and cellular endocrinology · 1996
Key publication · disorder Median craioencephalic dysraphias and olfactogenital dysplasia.World neurology · 1962
Manually curated
Association Review

In brief

The association between NR0B1 (Nuclear Receptor Subfamily 0 Group B Member 1) and Kallmann Syndrome is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 45
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

1 source

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

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03
NR0B1

The gene

1 source summary

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

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04
Kallmann Syndrome

The disorder

9 database identifiers

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

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05
Phenotype

Clinical features

44 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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07
Literature

Reading

1 publication

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

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08
Provenance

References & sources

6 references

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

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