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Semilobar Holoprosencephaly

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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Semilobar Holoprosencephaly is related to holoprosencephaly 1 and craniosynostosis. An important gene associated with Semilobar Holoprosencephaly is FGF8 (Fibroblast Growth Factor 8), and among its related pathways/superpathways are Nervous system development and Signal Transduction. Affiliated tissues include brain and olfactory bulb, and related phenotypes are failure to thrive and short stature
Related ID：
MALACARDS：SML028

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Newborn
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18
283
--
SML028

Medical Symptom

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

Gene & Mutation

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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!
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