Lymphatic Malformation 5 (LMPHM5)

Alias:
Meige Lymphedema
Meige Disease
Lymphedema Praecox
Meige Syndrome
Hereditary Lymphedema Type Ii
Lymphedema, Late-Onset
Late-Onset Lymphedema
Meigs Syndrome
Lmph2
Lymphedema, Hereditary, Ii, Formerly
Lymphedema, Hereditary, Ii
Lymphedema, Hereditary, 2
Hereditary Lymphedema Ii
Demons-Meigs Syndrome
Lmph2, Formerly
Meige's Disease
Lmphm5
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Lymphatic Malformation 5, also known as meige lymphedema, is related to lymphatic malformation 1 and yellow nail syndrome. An important gene associated with Lymphatic Malformation 5 is EPHB4 (EPH Receptor B4), and among its related pathways/superpathways is Neovascularisation processes. The drugs Acetylcholine and Cholinergic Agents have been mentioned in the context of this disorder. Affiliated tissues include skin and ovary, and related phenotypes are lymphedema and atypical scarring of skin
Related ID:
MESH:D008209
ICD11:1050919535

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
--
19
135
20

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