Hypogonadotropic Hypogonadism 1 with or Without Anosmia (HH1)

Alias:
Dysplasia Olfactogenitalis of De Morsier
Kallmann Syndrome 1
Hypogonadotropic Hypogonadism and Anosmia
Anosmic Hypogonadism
Kms
Kal1
Hh1
Hha
Hypogonadism, Hypogonadotropic, Type 1, with/without Anosmia
Hypogonadotropic Hypogonadism-Anosmia
Kallmann Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypogonadotropic Hypogonadism 1 with or Without Anosmia, also known as dysplasia olfactogenitalis of de morsier, is related to hypogonadotropic hypogonadism 2 with or without anosmia and hypogonadotropic hypogonadism 23 with or without anosmia. An important gene associated with Hypogonadotropic Hypogonadism 1 with or Without Anosmia is ANOS1 (Anosmin 1), and among its related pathways/superpathways is Kallmann syndrome. The drugs Zinc cation and Urofollitropin have been mentioned in the context of this disorder. Affiliated tissues include pituitary and hypothalamus, and related phenotypes are facial asymmetry and micropenis
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XL
XLD
Unknown
--
3
11
69

Medical Symptom

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No data available

Gene & Mutation

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MGI
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References Literature

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