Hypogonadotropic Hypogonadism 2 with or Without Anosmia (HH2)

Alias:
Kallmann Syndrome 2
Kal2
Hh2
Hypogonadism, Hypogonadotropic, Type 2 with/without Anosmia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypogonadotropic Hypogonadism 2 with or Without Anosmia, also known as kallmann syndrome 2, is related to hypogonadotropic hypogonadism 1 with or without anosmia and hypogonadism. An important gene associated with Hypogonadotropic Hypogonadism 2 with or Without Anosmia is FGFR1 (Fibroblast Growth Factor Receptor 1), and among its related pathways/superpathways are Signal Transduction and Signaling by Receptor Tyrosine Kinases. Affiliated tissues include pituitary and olfactory bulb, and related phenotypes are agenesis of corpus callosum and osteopenia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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16
155
91

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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