Log In|Sign Up
ENMeckel Syndrome 12 (MKS12)
Alias:
Lethal Fetal Cerebrorenogenitourinary Agenesis/hypoplasia Syndrome
Mks12
Meckel Syndrome, Type 12
Favorite
Meckel Syndrome 12, is also known as lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome. An important gene associated with Meckel Syndrome 12 is KIF14 (Kinesin Family Member 14). Affiliated tissues include occipital lobe and brain, and related phenotypes are microcephaly and intrauterine growth retardation
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
