Log In|Sign Up
ENThyroid Dyshormonogenesis 2a (TDH2A)
Alias:
Deficiency of Iodide Peroxidase
Iodide Peroxidase Deficiency
Tdh2a
Genetic Defect in Thyroid Hormonogenesis 2a
Thyroid Peroxidase Deficiency
Congenital Hypothyroidism Due to Dyshormonogenesis Type 2a
Hypothyroidism, Congenital, Due to Dyshormonogenesis, 2a
Thyroid Hormonogenesis, Genetic Defect in, 2a
Thyroid Dyshormonogenesis, Type 2a (tdh-2a_
Thyroid Hormone Organification Defect 2
Chdh2a
Tiod
Favorite
Thyroid Dyshormonogenesis 2a, also known as deficiency of iodide peroxidase, is related to congenital hypothyroidism and goiter. An important gene associated with Thyroid Dyshormonogenesis 2a is TPO (Thyroid Peroxidase), and among its related pathways/superpathways are Neuroscience and G alpha (s) signalling events. Affiliated tissues include thyroid and liver, and related phenotypes are hypothyroidism and goiter
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
