Cyagen
Tsing hua
Home
Toolbox
Resource
Workflow
TutorialsCitationsDownloads
News & Insights
Genetic EncyclopediaFrontiersIndustry InsightsCase Studies
About Us
About the SiteContact UsPrivate PolicyUser Agreement
Log In|Sign Up
EN

Hypomyelinating Leukodystrophy 8 (HLD8)

Alias:
Hypomyelinating Leukodystrophy 8 with or Without Oligodontia and-or Hypogonadotropic Hypogonadism
Hld8
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypomyelinating Leukodystrophy 8, also known as hld8, is related to leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism and leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism. An important gene associated with Hypomyelinating Leukodystrophy 8 is AVPR2 (Arginine Vasopressin Receptor 2). Related phenotype is integument.
Related ID：
MALACARDS：HYP902

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Unknown
--
5
46
--
HYP902

Medical Symptom

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

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top