Log In|Sign Up
ENMullerian Aplasia and Hyperandrogenism (MULLAPL)
Alias:
Mullerian Duct Failure and Hyperandrogenism
Wnt4 Deficiency
Mayer-Rokitansky-Küster-Hauser-Biason-Lauber Syndrome
Wnt4 Müllerian Aplasia and Ovarian Dysfunction
Wnt4 Mullerian Aplasia and Ovarian Dysfunction
Mayer-Rokitansky-Küster-Hauser-Like Syndrome
Müllerian Aplasia and Hyperandrogenism
Müllerian Duct Failure
Biason-Lauber Syndrome
Wnt4 Müllerian Aplasia
Mullapl
Favorite
Mullerian Aplasia and Hyperandrogenism, also known as mullerian duct failure and hyperandrogenism, is related to mayer-rokitansky-kuster-hauser syndrome and müllerian aplasia. An important gene associated with Mullerian Aplasia and Hyperandrogenism is WNT4 (Wnt Family Member 4), and among its related pathways/superpathways are Signal Transduction and Class A/1 (Rhodopsin-like receptors). Affiliated tissues include uterus and cervix, and related phenotypes are short stature and acne
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
