Autoimmune Polyendocrine Syndrome, Type Ii (APS2)

Alias:
Autoimmune Polyendocrine Syndrome Type 2
Schmidt Syndrome
Aps2
Autoimmune Thyroid Disease and/or Type 1 Diabetes-Addison Disease Syndrome
Autoimmune Polyglandular Syndrome Type 2
Autoimmune Polyendocrinopathy Type 2
Aps Type 2
Diabetes Mellitus, Addison Disease, Myxedema
Polyglandular Autoimmune Syndrome, Type Ii
Polyendocrine Autoimmune Syndrome, Type Ii
Autoimmune Syndrome Type Ii, Polyglandular
Autoimmune Syndrome Type Ii Polyglandular
Pga Ii
Aps Ii
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Autoimmune Polyendocrine Syndrome, Type Ii, also known as autoimmune polyendocrine syndrome type 2, is related to autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia and autoimmune polyendocrine syndrome type 1. An important gene associated with Autoimmune Polyendocrine Syndrome, Type Ii is GAD2 (Glutamate Decarboxylase 2), and among its related pathways/superpathways are 4-aminobutyrate degradation and Antipsychotics Pathway (Metabolic Side Effects), Pharmacodynamics. Affiliated tissues include thyroid and skin, and related phenotypes are type i diabetes mellitus and hashimoto thyroiditis

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
Adult
--
13
163
16

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
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