Hyperthyroxinemia

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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hyperthyroxinemia is related to thyroid hormone resistance, generalized, autosomal dominant and amyloidosis, hereditary, transthyretin-related. An important gene associated with Hyperthyroxinemia is SERPINA7 (Serpin Family A Member 7), and among its related pathways/superpathways are Angiopoietin-like protein 8 regulatory pathway and Transcription_Role of VDR in regulation of genes involved in osteoporosis. Affiliated tissues include thyroid and pituitary, and related phenotypes are limbs/digits/tail and homeostasis/metabolism
Related ID:
MESH:D006981

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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10
119
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Medical Symptom

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

Gene & Mutation

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Mutations
No data available

Related Drugs

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Phase
No data available

Disease Model

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MGI
Related Gene
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Publications
No data available

References Literature

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