Hyperthyroxinemia, Familial Dysalbuminemic (FDAH)

Alias:
Hyperthyroxinemia, Dysalbuminemic
Dysalbuminemic Hyperthyroxinemia
Bisalbuminemia
Fdah
Dysalbuminemic Hypertriiodothyroninemia
Euthyroid Hyperthyroxinemia 1
Fdh
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hyperthyroxinemia, Familial Dysalbuminemic, also known as hyperthyroxinemia, dysalbuminemic, is related to focal dermal hypoplasia and osteopathia striata with cranial sclerosis. An important gene associated with Hyperthyroxinemia, Familial Dysalbuminemic is ALB (Albumin). Affiliated tissues include thyroid and liver, and related phenotypes are euthyroid hyperthyroxinemia and increased circulating free t4 concentration
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
1
15
22

Medical Symptom

#
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
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Comparison
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