Frontonasal Dysplasia 1 (FND1)

Alias:
Frontonasal Dysplasia
Frontorhiny
Frontonasal Malformation
Midline Facial Cleft
Fnd
Fnm
Frontonasal Dysplasia Sequence
Median Facial Cleft Syndrome
Median Cleft Face Syndrome
Fnd1
Tessier Number 0-14 and 30 Facial Cleft
Isolated Median Cleft Face Syndrome
Alx3-Related Frontonasal Dysplasia
Frontonasal Dysplasia Type 1
Dysplasia, Frontonasal, Type
Median Cleft Syndrome
Median Facial Cleft
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Frontonasal Dysplasia 1, also known as frontonasal dysplasia, is related to craniofrontonasal syndrome and widow's peak. An important gene associated with Frontonasal Dysplasia 1 is ALX3 (ALX Homeobox 3). Affiliated tissues include bone and brain, and related phenotypes are scoliosis and ptosis
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Antenatal
1-9/1000000
21
114
19

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!
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