Permanent Congenital Hypothyroidism

Alias:
Congenital Hypothyroidism with Diffuse Goitre
Congenital Nontoxic Parenchymatous Goitre
Congenital Hypothyroidism Without Goitre
Congenital Thyroid Gland Insufficiency
Congenital Parenchymatous Struma
Congenital Parenchymatous Goitre
Congenital Thyroid Insufficiency
Thyroid Atrophy with Cretinism
Congenital Atrophy of Thyroid
Congenital Substernal Goitre
Congenital Nontoxic Goitre
Congenital Plunging Goitre
Congenital Thyroid Aplasia
Congenital Thyroid Atrophy
Congenital Diffuse Goitre
Congenital Diffuse Struma
Congenital Subthyroidism
Congenital Goitre Nos
Aplasia of Thyroid
Congenital Struma
Goitrous Cretin
Neonatal Struma
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Permanent Congenital Hypothyroidism, also known as congenital hypothyroidism with diffuse goitre, is related to primary congenital hypothyroidism and central congenital hypothyroidism. Affiliated tissues include thyroid and tongue.
Related ID:
ICD11:1756727158

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
1-5/10000
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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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