Related Conditions
Conditions Linked to Hypermobile EDS
hEDS affects the connective tissue that holds the body together — joints, blood vessels, skin, and organs. Because this tissue is present throughout the body, hEDS often occurs alongside other conditions.
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Autonomic Nervous System
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This is the part of the body that manages automatic functions such as heart rate, blood pressure, digestion, and temperature. In hEDS, this system doesn't always function as expected.
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Dysautonomia (General)
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This term describes irregularities in the autonomic nervous system that don't always fit a specific diagnosis.
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Signs: dizziness or lightheadedness, difficulty regulating body temperature, abnormal sweating, and digestive or bladder irregularities.
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Why it occurs: stretchier-than-typical connective tissue can affect the nerves and blood vessels this system relies on.
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POTS
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POTS (Postural Orthostatic Tachycardia Syndrome) means the heart rate rises abnormally upon standing.
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Signs: a racing heart, dizziness, lightheadedness, and fatigue after standing.
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Why it occurs: looser blood vessels make it harder for the body to maintain normal blood flow when changing position. Roughly six in ten people with POTS also meet criteria for hEDS or a related condition.
Immune System
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MCAS (Mast Cell Activation Syndrome)
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Mast cells are immune cells that release chemicals such as histamine — the same chemical involved in allergic reactions. In MCAS, they are triggered too easily.
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Signs: flushing, itching, hives, digestive upset, or nasal congestion, often triggered by heat, exercise, stress, or certain foods.
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Why it occurs: mast cells reside throughout connective tissue, so a body-wide difference in that tissue may make them more reactive.
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Note: hEDS, POTS, and MCAS frequently occur together — sometimes referred to as "the trifecta." This pattern is well recognized clinically, though researchers are still working out exactly why these three conditions are connected.
Brain and Spine
Craniocervical Instability (CCI)
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This occurs when the ligaments connecting the skull to the spine are looser than typical.
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Signs: severe headaches and neck pain, a heavy or unstable feeling in the head, dizziness, blurred vision, ringing in the ears, and brain fog.
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Why it occurs: the same ligament laxity responsible for joint hypermobility elsewhere can also affect the neck.
Chiari Malformation and Tethered Cord Syndrome
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Both involve the brain or spinal cord not being positioned as expected.
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Signs: lower back pain, balance difficulties, leg weakness, or bladder and bowel issues (tethered cord); symptoms often overlap with those of CCI.
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Why it occurs: loose connective tissue can affect the structures supporting the spinal cord. These conditions are less common than POTS or MCAS and typically require specialized imaging to diagnose.
Joints and Muscles
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TMJ (Jaw) Dysfunction
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The jaw is a joint like any other, so it can be affected by the same hypermobility seen elsewhere in the body.
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Signs: jaw pain, clicking, locking, or difficulty chewing.​​​
Digestive System
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The gut contains substantial connective tissue and its own nervous system, so it is frequently affected.
Slow digestion
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Food moves through the gut more slowly than typical, which can cause bloating, nausea, or irregular bowel habits.
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Reflux and swallowing difficulty:
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Heartburn and trouble swallowing occur more frequently in hEDS.
Pelvic and Bladder
Pelvic floor dysfunction
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Looser tissue can make it harder for the pelvic floor to support pelvic organs, sometimes resulting in prolapse or incontinence.
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Bladder pain
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Chronic bladder pain and frequent urinary urgency occur more often in hEDS.
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Endometriosis
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Many people with hEDS also have endometriosis, and the two conditions share symptoms such as pelvic pain and painful periods. The evidence for a direct biological link is mixed, however — some studies find a higher prevalence, while others do not find a significant association. Because the symptoms overlap so closely, one condition is sometimes mistaken for the other.
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Other Common Conditions
Chronic pain
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Chronic pain is common in hEDS, often stemming from repeated joint injuries or from the body's pain-processing system becoming more sensitive over time.
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Signs: widespread aching, fatigue, poor sleep, and pain that seems disproportionate to any single injury. This closely resembles fibromyalgia, even though the underlying cause is connective tissue laxity.
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Migraine
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Headaches tend to occur more frequently and with greater severity
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Raynaud's phenomenon
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Fingers or toes turn white or blue in response to cold or stress.
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Sleep difficulties
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Trouble falling or staying asleep, often worsened by pain or autonomic symptoms.
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Persistent fatigue
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Profound, disproportionate tiredness that overlaps with ME/CFS (chronic fatigue syndrome).
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Anxiety and mood changes
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Living with a complex, often invisible condition is genuinely difficult. Researchers are also examining whether the nervous system itself contributes to anxiety-like symptoms in hEDS — this appears to be a two-way relationship, not an indication that the physical symptoms are simply psychological.
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Hypermobile EDS (hEDS) is the most common subtype, with symptoms often including joint hypermobility, chronic pain, and fragile, velvety skin that bruises easily. People with hEDS can be prone to subluxations and dislocations that occur spontaneously or on minimal impact. They can also have related conditions, including dysautonomia/POTS, Mast Cell Activation Syndrome (MCAS), gastrointestinal dysmotility, and chronic fatigue. The Norris Lab's recent global study found that hEDS patients surveyed had an average of 24 co-occurring conditions.
Hypermobile EDS is considered a genetic condition. However, scientists are still in the process of identifying genes that impact the condition; at this time, there is no reliable genetic testing available for hEDS. Instead, the diagnostic process relies on clinical verification.

Vascular EDS (VEDS) is a rare, serious connective tissue disorder. “Vascular” refers to the body’s system of blood vessels. People with VEDS have fragile arteries (blood vessels) and internal organs, putting them at high risk of severe bleeding, organ rupture, and other life-threatening complications. ​​​
​VEDS is caused by mutations (changes) in the gene that tells the body how to make collagen III, a protein that provides strength to blood vessels, the bowel, uterus, and other hollow organs. In people with VEDS, these genetic changes have serious consequences: their bodies do not produce enough collagen III, or the collagen III they make is faulty and does not function properly. When collagen III cannot do its job, blood vessels and other organs can become severely fragile.​
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Learn more about Vascular EDS and available resourcesat the VEDS Movement.
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Collagen is a protein that provides structure and support to connective tissues, including skin, muscles, ligaments, tendons, and bones. People with EDS experience weakened connective tissues as a result of collagen abnormalities. Connective tissues are everywhere in the body. This means EDS is complex and typically affects multiple body systems at once.
There are currently 13 recognized subtypes of EDS. They are classified based on clinical features, genes affected, and pattern of inheritance:
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Arthrochalasia EDS (aEDS)
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Brittle cornea syndrome (BCS)
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Cardiac valvular EDS (cvEDS)

Custom ring splints created by OT Donna VanHelene offer support for hypermobile fingers

There are currently 13 recognized subtypes of EDS. They are classified based on clinical features, genes affected, and pattern of inheritance:
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Arthrochalasia EDS (aEDS)
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Brittle cornea syndrome (BCS)
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Cardiac valvular EDS (cvEDS)

Sources
Alomari, M., Hitawala, A., Chadalavada, P., Covut, F., Al Momani, L., Khazaaleh, S., Gosai, F., Al Ashi, S., Abushahin, A., & Schneider, A. (2020). Prevalence and predictors of gastrointestinal dysmotility in patients with hypermobile Ehlers-Danlos syndrome: A tertiary care center experience. Cureus, 12(4), e7881. https://doi.org/10.7759/cureus.7881 Daylor, V., Griggs, M., Weintraub, A., Byrd, R., Petrucci, T., Huff, M., Byerly, K., Fenner, R., Severance, S., Griggs, C., Sharma, A., Atwal, P., Kautz, S. A., Shapiro, S., Youkhana, K., Lavallee, M., Wilkerson, A., Nichols, M., Snyder, A., Eichinger, J. K., Patel, S., Maitland, A., Gensemer, C., & Norris, R. A. (2025). Defining the chronic complexities of hEDS and HSD: A global survey of diagnostic challenges, life-long comorbidities, and unmet needs. Journal of Clinical Medicine, 14(16), Article 5636. https://doi.org/10.3390/jcm14165636 Gilliam, E., Hoffman, J. D., & Yeh, G. (2019). Urogenital and pelvic complications in the Ehlers-Danlos syndromes and associated hypermobility spectrum disorders: A scoping review. Clinical Genetics, 97(1), 1–11. Henderson, F. C., Sr., Austin, C., Benzel, E., Bolognese, P., Ellenbogen, R., Francomano, C. A., Ireton, C., Klinge, P., Koby, M., Long, D., Patel, S., Singman, E. L., & Voermans, N. C. (2017). Neurological and spinal manifestations of the Ehlers-Danlos syndromes. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 175(1), 195–211. Hugon-Rodin, J., Lebègue, G., Becourt, S., Hamonet, C., & Gompel, A. (2016). Gynecologic symptoms and the influence on reproductive life in 386 women with hypermobility type Ehlers-Danlos syndrome: A cohort study. Orphanet Journal of Rare Diseases, 11, Article 124. https://doi.org/10.1186/s13023-016-0511-2 Kohn, A., & Chang, C. (2020). The relationship between hypermobile Ehlers-Danlos syndrome (hEDS), postural orthostatic tachycardia syndrome (POTS), and mast cell activation syndrome (MCAS). Clinical Reviews in Allergy & Immunology, 58(3), 273–297. https://doi.org/10.1007/s12016-019-08755-8 Miller, A. J., Stiles, L. E., Sheehan, T., Bascom, R., Levy, H. P., Francomano, C., & Arnold, A. C. (2020). Prevalence of hypermobile Ehlers-Danlos syndrome in postural orthostatic tachycardia syndrome. Autonomic Neuroscience, 224, Article 102637. https://doi.org/10.1016/j.autneu.2019.102637 Wang, E., Ganti, T., Vaou, E., & Hohler, A. (2021). The relationship between mast cell activation syndrome, postural tachycardia syndrome, and Ehlers-Danlos syndrome. Allergy and Asthma Proceedings, 42(3), 243–246. https://doi.org/10.2500/aap.2021.42.210022
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