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adenoma","onset_id":null,"reference":"ORPHA:552","source_release":"2026-06-23"},"sourceGroups":["orphanet"]},{"frequencyKind":"range","key":"fec930a4db98da3ed8dbf5e72817c5e519808c4fad5d1ce9c587ebb6d97cbb33","raw":{"aspect":"P","body_system":"blood","disease_id":"ORPHA:552","disease_name":"MODY","evidence":"TAS","frequency_raw":"HP:0040282","hpo_id":"HP:0040217","is_excluded":false,"label":"Elevated hemoglobin A1c","onset_id":null,"reference":"ORPHA:552","source_release":"2026-06-23"},"sourceGroups":["orphanet"]}],"referenceLabels":{},"references":{"causeHtml":"<ul><li><a href=\"https://medlineplus.gov/genetics/condition/maturity-onset-diabetes-of-the-young\">Maturity-onset diabetes of the young</a></li></ul>","identityNote":"MONDO cross-references identify native condition entries. Ancestor membership does not transfer phenotype values between groups.","importantHtml":""},"sections":[{"bodyHtml":"<p>MODY can be caused by a mutation in one of several genes. HNF1A-MODY, GCK-MODY, HNF4A-MODY, and RCAD, are caused by mutations in the HNF1A, GCK, HNF4A, and HNF1B gene, respectively. All of these genes provide instructions for making proteins involved in the production of insulin to control blood glucose levels in the body. In particular, the proteins are important in specialized cells in the pancreas called beta cells, which secrete insulin.</p><p>The proteins produced from the HNF1A, HNF4A, and HNF1B genes all act as transcription factors, which means they control the activity of other genes. In particular, these proteins regulate genes that direct the development and function of beta cells. HNF1A, HNF4A, or HNF1B gene mutations result in production of an altered transcription factor that is unable to function normally. These changes alter gene activity in cells, impairing normal beta cell development and function. As a result, beta cells are less able than normal to produce insulin in response to glucose in the blood, which means the body cannot control blood glucose. Elevated blood glucose results in the signs and symptoms of MODY. Some of these MODY-related genes play roles in the development of other body systems, in addition to beta cells. Disrupted development of these systems underlies additional signs and symptoms in particular forms of MODY. For example, the HNF1B gene is involved in kidney development, which helps explain the kidney abnormalities in people with RCAD.</p><p>The protein produced from the GCK gene acts as a sensor that recognizes when the amount of glucose in the blood rises. In response, the protein helps stimulate the release of insulin from beta cells so glucose can be taken up and used by cells for energy. This protein also helps determine when excess glucose should be taken into liver cells and stored. Mutations in the GCK gene limit the protein&#x27;s ability to sense a rise in blood glucose, so levels remain elevated.</p><p>Other genes involved in controlling blood glucose cause rare types of MODY. It is likely that additional genes that have not been identified are also involved in the condition.</p><p class=\"section-source\"><a href=\"https://medlineplus.gov/genetics/condition/maturity-onset-diabetes-of-the-young/#causes\">MedlinePlus Genetics: Causes</a></p>","key":"forms","title":"What causes Maturity-onset diabetes of the young?"},{"bodyHtml":"<p>The different types of MODY are distinguished by their genetic causes. The most common types are HNF1A-MODY (also known as MODY3), accounting for 50 to 70 percent of cases, and GCK-MODY (MODY2), accounting for 30 to 50 percent of cases. Less frequent types include HNF4A-MODY (MODY1) and renal cysts and diabetes (RCAD) syndrome (also known as HNF1B-MODY or MODY5), which each account for 5 to 10 percent of cases. At least ten other types have been identified, and these are very rare.</p><p>HNF1A-MODY and HNF4A-MODY have similar signs and symptoms that develop slowly over time. Early signs and symptoms in these types are caused by high blood glucose and may include frequent urination (polyuria), excessive thirst (polydipsia), fatigue, blurred vision, weight loss, and recurrent skin infections. Over time uncontrolled high blood glucose can damage small blood vessels in the eyes and kidneys. Damage to the light-sensitive tissue at the back of the eye (the retina) causes a condition known as diabetic retinopathy that can lead to vision loss and eventual blindness. Kidney damage (diabetic nephropathy) can lead to kidney failure and end-stage renal disease (ESRD). While these two types of MODY are very similar, certain features are particular to each type. For example, babies with HNF4A-MODY tend to weigh more than average or have abnormally low blood glucose at birth, even though other signs of the condition do not occur until childhood or young adulthood. People with HNF1A-MODY have a higher-than-average risk of developing noncancerous (benign) liver tumors known as hepatocellular adenomas.</p><p>GCK-MODY is a very mild type of the condition. People with this type have slightly elevated blood glucose levels, particularly in the morning before eating (fasting blood glucose). However, affected individuals often have no symptoms related to the disorder, and diabetes-related complications are extremely rare.</p><p>RCAD is associated with a combination of diabetes and kidney or urinary tract abnormalities (unrelated to the elevated blood glucose), most commonly fluid-filled sacs (cysts) in the kidneys. However, the signs and symptoms are variable, even within families, and not everyone with RCAD has both features. Affected individuals may have other features unrelated to diabetes, such as abnormalities of the pancreas or liver or a form of arthritis called gout.</p><p class=\"section-source\">Source: <a href=\"https://medlineplus.gov/genetics/condition/maturity-onset-diabetes-of-the-young\">MedlinePlus Genetics</a></p>","key":"overview","title":"Condition overview"}],"sharedSources":[],"slug":"maturity-onset-diabetes-of-the-young","sourceDocuments":[{"name":"Maturity-onset diabetes of the young","reviewed":"2020-07","sections":{"causes":{"fetchedAt":"2026-10-20T20:23:07.730577+00:00","label":"Causes","pageSha256":"cfdca7ff1485693d5fa5a64e68cb33aa45a967519cb541718e9b571dbfd04bfd","sourceUrl":"https://medlineplus.gov/genetics/condition/maturity-onset-diabetes-of-the-young/#causes","status":"available"}},"source_release":"2026-10-01","url":"https://medlineplus.gov/genetics/condition/maturity-onset-diabetes-of-the-young"}],"sourceNote":"MedlinePlus descriptions and Causes; original HPO annotations.","takeawayHtml":"Cause explanations are from MedlinePlus Genetics. Feature values below retain their original sources and patient groups.","title":"Maturity-onset diabetes of the young"},"schemaVersion":1}