Disease Browser
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Parent Node: Diabetes Mellitus, Type 2 (D003924) | ..Starting node ..Mason-Type Diabetes (C562772)
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Sister Nodes: | ..Diabetes Mellitus, Lipoatrophic (D003923) 1
| ..Diabetes Mellitus, Noninsulin-Dependent, 1 (C563359)
| ..Diabetes Mellitus, Noninsulin-Dependent, 2 (C563323)
| ..Diabetes Mellitus, Noninsulin-Dependent, 3 (C566342)
| ..Diabetes Mellitus, Noninsulin-Dependent, Type 4 (C564299)
| ..Diabetes Mellitus, Type II, Autosomal Dominant (C562773)
| ..Mason-Type Diabetes (C562772)
| ..Maturity-Onset Diabetes of the Young, Type 1 (C565101)
| ..Maturity-Onset Diabetes of the Young, Type 2 (C564219)
| ..Maturity-Onset Diabetes of the Young, Type 3 (C563933)
| ..Maturity-Onset Diabetes of the Young, Type 4 (C563451)
| ..Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction (C565225)
| ..Maturity-Onset Diabetes Of The Young, Type 9 (C567393)
| ..MODY, Type 6 (C565231)
| ..Noninsulin-dependent diabetes mellitus with deafness (C536246)
| ..Renal cysts and diabetes syndrome (C535520)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 6811 |
Name: | Mason-Type Diabetes |
Definition: | |
Alternative IDs: | OMIM:606391 |
ParentIDs: | MESH:D003924 |
TreeNumbers: | C18.452.394.750.149/C562772 |C19.246.300/C562772 |
Synonyms: | MASON-TYPE DIABETES |Maturity-Onset Diabetes of the Young |MODY |
Slim Mappings: | Endocrine system disease|Metabolic disease |
Reference: |
MedGen: C562772
MeSH: C562772
OMIM: 606391;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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