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Hypogonadotropic Hypogonadism 1 With Or Without Anosmia (MONDO:0010635)

The X-linked inherited form of Kallmann syndrome caused by mutation of the KAL1 gene mapped to chromosome Xp22.3.

Overview

Category

Ontology ID

Internal:11781

Synonyms

ANOS1 hypogonadotropic hypogonadism

hypogonadotropic hypogonadism 1 with or without anosmia

hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), X-linked recessive

hypogonadotropic hypogonadism caused by mutation in ANOS1

HH1

KAL1

KMS

Kallmann syndrome 1

Kallmann syndrome, X-linked

Kallmann syndrome, type 1, X-linked

anosmic hypogonadism

dysplasia Olfactogenitalis of De Morsier

hypogonadotropic hypogonadism and anosmia

Mapped terms

DOID:0090094

GARD:0003071

MEDGEN:295872

NCIT:C75480

OMIM:308700

UMLS:C1563719

Child terms

Unknown children.