Leydig Cell Hypoplasia Type Ii

Alias:
46,xy Disorder of Sex Developement Due to Partial Luteinizing Hormone Resistance
Leydig Cell Hypoplasia Due to Partial Luteinizing Hormone Receptor Inactivation
46,xy Disorder of Sex Developement Due to Partial Lh Receptor Inactivation
Leydig Cell Hypoplasia Due to Partial Luteinizing Hormone Resistance
46,xy Disorder of Sex Developement Due to Partial Lh Resistance
Leydig Cell Hypoplasia Due to Partial Lh Receptor Inactivation
46,xy Dsd Due to Partial Luteinizing Hormone Resistance
Leydig Cell Hypoplasia Due to Partial Lh Resistance
46,xy Dsd Due to Partial Lh Receptor Inactivation
46,xy Dsd Due to Partial Lh Resistance
Leydig Cell Hypoplasia, Type Ii
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Leydig Cell Hypoplasia Type Ii, also known as 46,xy disorder of sex developement due to partial luteinizing hormone resistance, is related to leydig cell hypoplasia, type i and leydig cell hypoplasia. An important gene associated with Leydig Cell Hypoplasia Type Ii is LHCGR (Luteinizing Hormone/Choriogonadotropin Receptor), and among its related pathways/superpathways are G-protein signaling_Rap2B regulation pathway and Hormone ligand-binding receptors. Related phenotypes are Decreased caspase 3/7 activity and liver/biliary system
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Newborn
--
6
23
3

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
Journal
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IF
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