MODY (maturity-onset diabetes of the young) is a rare, familial, clinically and genetically heterogeneous form of diabetes characterized by young age of onset (generally 10-45 years of age) with maintenance of endogenous insulin production, lack of pancreatic beta-cell autoimmunity, absence of obesity and insulin resistance and extra-pancreatic manifestations in some subtypes.
Synonyms:
Maturity-onset diabetes of the young
This is just here as a test because I lose it
Term information
database
cross reference
- OMIM:600496 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:125850 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- UMLS:C0342276 (E (Exact mapping: the two concepts are equivalent))
- OMIM:606391 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:616329 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:613375 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:616511 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:606392 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:606394 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:125851 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:610508 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:612225 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:613370 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- OMIM:609812 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- ICD-10:E13 (- NTBT (ORPHA code's Narrower Term maps to a Broader Term). - Attributed (The ICD10 code is attributed by Orphanet).)
definition citation
- Orphanet
expertlink
- https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=552
hasDbXref
- OMIM:610508
- OMIM:600496
- OMIM:609812
- OMIM:613370
- ICD-10:E13
- OMIM:125851
- OMIM:613375
- OMIM:616511
- OMIM:606391
- UMLS:C0342276
- OMIM:616329
- OMIM:612225
- OMIM:606392
- OMIM:125850
- OMIM:606394
has age of onset
- http://www.orpha.net/ORDO/Orphanet_409948
- http://www.orpha.net/ORDO/Orphanet_409947
- http://www.orpha.net/ORDO/Orphanet_409946
has inheritance
- http://www.orpha.net/ORDO/Orphanet_409929
- http://www.orpha.net/ORDO/Orphanet_409941
has point prevalence range
- http://www.orpha.net/ORDO/Orphanet_409975
notation
- ORPHA:552
part of
- http://www.orpha.net/ORDO/Orphanet_183625
- http://www.orpha.net/ORDO/Orphanet_181376
present in
- http://www.orpha.net/ORDO/Orphanet_410224
- http://www.orpha.net/ORDO/Orphanet_409984
Term relations
Subclass of:
Related from:
disease-causing germline mutation(s) in
- glucokinase
- pancreatic and duodenal homeobox 1
- Kruppel like factor 11
- carboxyl ester lipase
- HNF1 homeobox A
- potassium inwardly rectifying channel subfamily J member 11
- neuronal differentiation 1
- hepatocyte nuclear factor 4 alpha
- paired box 4
- insulin
- BLK proto-oncogene, Src family tyrosine kinase
- ATP binding cassette subfamily C member 8