Rare genetic diabetes mellitus

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Rare genetic diabetes mellitus

ORPHA:183625Category

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Classified as
Category

Genes reported in subtypes

ABCC8ALMS1APPL1BLKCASRCELCISD2CPA1CTRCDCAF17DNAJC3DUTEIF2AK3GATA6GCKHNF1AHNF1BHNF4AIER3IP1INSKCNJ11KLF11MT-TENEUROD1PAX4PDX1PPP1R15BPRSS1PRSS2SLC19A2SLC29A3TRMT10ATRPV6WFS1YIPF5

Orphanet records these genes on 17 more specific entries under this disorder, not on this entry itself:

Alström syndromeAtypical Fanconi syndrome-neonatal hyperinsulinism syndromeAutosomal dominant hereditary chronic pancreatitisBone marrow failure-diabetes mellitus syndromeHNF1B-related autosomal dominant tubulointerstitial kidney diseaseH syndromeJuvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndromeMODYMyopathy and diabetes mellitusPancreatic hypoplasia-diabetes-congenital heart disease syndromePrimary microcephaly-epilepsy-permanent neonatal diabetes syndromePrimary microcephaly-mild intellectual disability-young-onset diabetes syndromeThiamine-responsive megaloblastic anemia syndromeWolcott-Rallison syndromeWolfram-like syndromeWolfram syndromeWoodhouse-Sakati syndrome

A well-studied disease is usually split into subtypes, and the gene is curated on whichever one the evidence belongs to. Open a subtype to see which gene goes with it.

Cross-references

MONDO 15967UMLS C5680537

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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