Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome

Alias:
Fatco Syndrome
Fibular Aplasia-Tibial Campomelia-Oligosyndactyly Syndrome
Hecht-Scott Syndrome
Hecht Scott Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome, also known as fatco syndrome, is related to brachydactyly-ectrodactyly with fibular aplasia or hypoplasia and fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly. Affiliated tissues include bone, and related phenotypes are absent hand and abnormal fibula morphology

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Antenatal
<1/1000000
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--
5

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

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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