Genopathy
Gene-Disorder Association · Article
Gene
SEMA7A
Semaphorin 7A (JohnMiltonHagen Blood Group)
Disorder
Hypogonadotropic Hypogonadism 14 With Or Without Anosmia
First reported 1990
Key publication · disorder Macrophage-like cells in the presumptive optic pathways in the floor of the diencephalon of the chick embryo.Journal of neurocytology · 1990
Manually curated
Association Review

In brief

The association between SEMA7A (Semaphorin 7A (JohnMiltonHagen Blood Group)) and Hypogonadotropic Hypogonadism 14 With Or Without Anosmia is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 14
Compounds 0
Trials 0
Publications 0
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
SEMA7A

The gene

1 source summary

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

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04
Hypogonadotropic Hypogonadism 14 With Or Without Anosmia

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

5 clinical features

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

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06
Provenance

References & sources

4 references

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

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