Midline Interhemispheric Variant of Holoprosencephaly (MIH)

Alias:
Middle Interhemispheric Variant of Holoprosencephaly
Middle Interhemispheric Fusion Variant
Syntelencephaly
Mih Type Hpe
Mihf
Mihv
Mih
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Midline Interhemispheric Variant of Holoprosencephaly, also known as middle interhemispheric variant of holoprosencephaly, is related to holoprosencephaly 1 and cleft palate, isolated. An important gene associated with Midline Interhemispheric Variant of Holoprosencephaly is CDON (Cell Adhesion Associated, Oncogene Regulated), and among its related pathways/superpathways are Signal Transduction and Nervous system development. Affiliated tissues include hypothalamus and brain, and related phenotypes are failure to thrive and short stature
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Newborn
1-9/100000
14
217
--

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