Hypogonadotropic Hypogonadism 5 with or Without Anosmia (HH5)

Alias:
Kallmann Syndrome 5
Hh5
Hypogonadism, Hypogonadotropic, Type 5 with/without Anosmia
Hypogonadotropic Hypogonadism 5 Without Anosmia
Kal5
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypogonadotropic Hypogonadism 5 with or Without Anosmia, also known as kallmann syndrome 5, is related to hypogonadotropic hypogonadism 2 with or without anosmia and esophageal atresia. An important gene associated with Hypogonadotropic Hypogonadism 5 with or Without Anosmia is CHD7 (Chromodomain Helicase DNA Binding Protein 7). Affiliated tissues include pituitary and ovary, and related phenotypes are anosmia and sensorineural hearing impairment
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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10
72
14

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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