Arthritis, and Vertigo

Diseases related with Arthritis and Vertigo

In the following list you will find some of the most common rare diseases related to Arthritis and Vertigo that can help you solving undiagnosed cases.


Top matches:

Medium match TUMOR NECROSIS FACTOR RECEPTOR 1 ASSOCIATED PERIODIC SYNDROME


Tumor necrosis factor receptor 1 associated periodic syndrome (TRAPS) is a periodic fever syndrome, characterized by recurrent fever, arthralgia, myalgia and tender skin lesions lasting for 1 to 3 weeks, associated with skin, joint, ocular and serosal inflammation and complicated by secondary amyloidosis (see this term).

TUMOR NECROSIS FACTOR RECEPTOR 1 ASSOCIATED PERIODIC SYNDROME Is also known as tnf receptor 1-associated periodic syndrome|fpf|traps syndrome|hibernian fever, familial|familial hibernian fever|fhf|tnf receptor-associated periodic syndrome|tumor necrosis factor receptor-associated periodic syndrome|traps

Related symptoms:

  • Neoplasm
  • Pain
  • Anemia
  • Fever
  • Edema


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about TUMOR NECROSIS FACTOR RECEPTOR 1 ASSOCIATED PERIODIC SYNDROME

Medium match GIANT CELL ARTERITIS


Giant cell arteritis (GCA) is a large vessel vasculitis predominantly involving the arteries originating from the aortic arch and especially the extracranial branches of the carotid arteries.

GIANT CELL ARTERITIS Is also known as horton disease|giant cell arteritis|temporal arteritis|cranial arteritis|polymyalgia rheumatica|gca

Related symptoms:

  • Hearing impairment
  • Ataxia
  • Nystagmus
  • Muscle weakness
  • Ptosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about GIANT CELL ARTERITIS

Medium match EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE


Ehlers-Danlos syndrome, hypermobility type (HT-EDS) is the most frequent form of EDS (see this term), a group of hereditary connective tissue diseases, and is characterized by joint hyperlaxity, mild skin hyperextensibility, tissue fragility and extra-musculoskeletal manifestations.

EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE Is also known as benign joint hypermobility syndrome|ehlers-danlos syndrome, hypermobile type|ht-eds|ehlers-danlos syndrome, type iii|benign hypermobility syndrome|ehlers-danlos syndrome type 3|eds iii|eds3|bjhs

Related symptoms:

  • Scoliosis
  • Pain
  • Ptosis
  • Epicanthus
  • Fatigue


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE

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Other less relevant matches:

Medium match HYPERIMMUNOGLOBULINEMIA D WITH PERIODIC FEVER


Hyperimmunoglobinemia D with periodic fever (HIDS) is a rare autoinflammatory disease characterized by periodic attacks of fever and a systemic inflammatory reaction (cervical lymphadenopathy, abdominal pain, vomiting, diarrhea, arthralgias and skin signs).

HYPERIMMUNOGLOBULINEMIA D WITH PERIODIC FEVER Is also known as hyperimmunoglobinemia d with recurrent fever|hyper-igd syndrome|hyperimmunoglobulinemia d and periodic fever syndrome|partial mevalonate kinase deficiency|hids|periodic fever, dutch type|hyperimmunoglobulinemia d syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Microcephaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about HYPERIMMUNOGLOBULINEMIA D WITH PERIODIC FEVER

Medium match BEHÇET DISEASE


Behçet's disease (BD) is a chronic, relapsing, multisystemic vasculitis characterized by mucocutaneous lesions, as well as articular, vascular, ocular and central nervous system manifestations.

BEHÇET DISEASE Is also known as bd|behcet disease

Related symptoms:

  • Seizures
  • Ataxia
  • Neoplasm
  • Pain
  • Cataract


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about BEHÇET DISEASE

Medium match EHLERS-DANLOS SYNDROME, VASCULAR TYPE


Ehlers-Danlos syndrome type IV, also known as the vascular type of Ehlers-Danlos syndrome (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial, digestive and uterine complications, which are rarely, if at all, observed in the other forms of EDS.

EHLERS-DANLOS SYNDROME, VASCULAR TYPE Is also known as ehlers-danlos syndrome, type iv, autosomal dominant|eds type 4|ehlers-danlos syndrome type 4|ehlers-danlos syndrome type iv|ehlers-danlos syndrome, ecchymotic type|ehlers-danlos syndrome, arterial type|eds4|sack-barabas syndrome|eds iv|ehlers-danlos syndr

Related symptoms:

  • Global developmental delay
  • Short stature
  • Hypertelorism
  • Pain
  • Cryptorchidism


SOURCES: ORPHANET OMIM MENDELIAN

More info about EHLERS-DANLOS SYNDROME, VASCULAR TYPE

Low match FABRY DISEASE


Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterized by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations.

FABRY DISEASE Is also known as ceramide trihexosidase deficiency|hereditary dystopic lipidosis|fd|alpha-galactosidase a deficiency|diffuse angiokeratoma|gla deficiency|angiokeratoma corporis diffusum|anderson-fabry disease

Related symptoms:

  • Seizures
  • Short stature
  • Hearing impairment
  • Sensorineural hearing impairment
  • Pain


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about FABRY DISEASE

Low match SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA; SEDC


Spondyloepiphyseal dysplasia congenita is an autosomal dominant chondrodysplasia characterized by disproportionate short stature (short trunk), abnormal epiphyses, and flattened vertebral bodies. Skeletal features are manifested at birth and evolve with time. Other features include myopia and/or retinal degeneration with retinal detachment and cleft palate (summary by Anderson et al., 1990).

SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA; SEDC Is also known as sed congenita|spondyloepiphyseal dysplasia, congenital type

Related symptoms:

  • Intellectual disability
  • Short stature
  • Generalized hypotonia
  • Hearing impairment
  • Scoliosis


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA; SEDC

Low match DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION; DFNA34


DFNA34 is an autosomal dominant form of postlingual, slowly progressive sensorineural hearing loss with variable severity and variable additional features. Some patients have pure hearing loss without significant additional features, whereas some patients have features of an autoinflammatory disorder with systemic manifestations, including periodic fevers, arthralgias, and episodic urticaria. The disorder results from abnormally increased activation of the inflammatory pathway, and treatment with an IL1 receptor antagonist (see {147679}) may be effective if started early (summary by Nakanishi et al., 2017).

Related symptoms:

  • Hearing impairment
  • Sensorineural hearing impairment
  • Fever
  • Edema
  • Headache


SOURCES: OMIM MENDELIAN

More info about DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION; DFNA34

Low match MITOCHONDRIAL NON-SYNDROMIC SENSORINEURAL DEAFNESS


Mutations in mitochondrial DNA (mtDNA) have been found to be associated with nonsyndromic sensorineural hearing loss. Matrilineal relatives within and among families carrying certain pathogenic mitochondrial mutations exhibit a wide range of penetrance, severity, and age of onset of hearing loss, indicating that the mitochondrial mutations by themselves are not sufficient to produce a deafness phenotype. Modifier factors, such as nuclear and mitochondrial genes, or environmental factors, such as exposure to aminoglycosides, appear to modulate the phenotypic manifestations (summary by Tang et al., 2007).

MITOCHONDRIAL NON-SYNDROMIC SENSORINEURAL DEAFNESS Is also known as isolated mitochondrial neurosensory deafness|isolated mitochondrial sensorineural deafness|mitochondrial non-syndromic neurosensory deafness

Related symptoms:

  • Hearing impairment
  • Sensorineural hearing impairment
  • Vertigo
  • Tinnitus


SOURCES: ORPHANET OMIM MENDELIAN

More info about MITOCHONDRIAL NON-SYNDROMIC SENSORINEURAL DEAFNESS

Top 5 symptoms//phenotypes associated to Arthritis and Vertigo

Symptoms // Phenotype % cases
Pain Common - Between 50% and 80% cases
Arthralgia Common - Between 50% and 80% cases
Paresthesia Common - Between 50% and 80% cases
Myalgia Common - Between 50% and 80% cases
Migraine Common - Between 50% and 80% cases
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Other less frequent symptoms

Patients with Arthritis and Vertigo. may also develop some of the following symptoms:

Common Symptoms - More than 50% cases


Headache

Uncommon Symptoms - Between 30% and 50% cases


Fever Hearing impairment Fatigue Abdominal pain Vasculitis Cataract Sensorineural hearing impairment Elevated erythrocyte sedimentation rate Subcutaneous nodule Nausea Cough Lymphadenopathy Papule Renal insufficiency Depressivity Dilatation Constipation Edema Vomiting Diarrhea Seizures Abnormal myocardium morphology Optic neuritis Tinnitus Anorexia Ataxia Glaucoma Hyperhidrosis Ptosis Alopecia Arrhythmia Hypertelorism Blindness Neoplasm Pericarditis Uveitis Conjunctivitis Behavioral abnormality Splenomegaly Hip dislocation Inguinal hernia Erythema Skin rash Short stature Nausea and vomiting Chest pain Hypertension Meningitis Scoliosis Malabsorption Stroke Limitation of joint mobility Osteoarthritis Mitral valve prolapse Abdominal distention

Rare Symptoms - Less than 30% cases


Cystocele Arterial dissection Gingival overgrowth Joint dislocation Abnormality of the gingiva Osteolysis Microdontia Joint hyperflexibility Acrocyanosis Transient ischemic attack Keratoconus Keratoconjunctivitis sicca Aortic root aneurysm Ascending tubular aorta aneurysm Gingivitis Thin skin Gastrointestinal dysmotility Aplasia/Hypoplasia of the abdominal wall musculature Progressive hearing impairment Purpura Intellectual disability Flat face Hemoptysis Glomerulopathy Cognitive impairment Rheumatoid arthritis Talipes equinovarus Respiratory insufficiency Aortic regurgitation Mitral regurgitation Myocardial infarction Autoimmunity Developmental regression Dyspnea Gait disturbance Cervical lymphadenopathy Global developmental delay Recurrent aphthous stomatitis Progressive sensorineural hearing impairment Abnormal intestine morphology Sleep apnea Urticaria Umbilical hernia Nephrotic syndrome Gastrointestinal hemorrhage Telangiectasia of the skin Abnormal heart valve morphology Flexion contracture Growth delay Generalized hypotonia Apnea Joint hypermobility Neuritis Congestive heart failure Cerebral ischemia Aortic dissection Gangrene Leukocytosis Peritonitis Diabetes insipidus Hypermelanotic macule Myositis Macule Erysipelas Visual loss Muscle weakness Optic disc pallor Midface retrusion Sudden cardiac death Episodic fever Peripheral neuropathy Hematuria Optic atrophy Joint stiffness Amyloidosis Arterial thrombosis Intestinal obstruction Cranial nerve paralysis Gastrointestinal infarctions Pleuritis Abnormality of the dentition Epicanthus Abnormal lung morphology Orchitis Chills Periorbital edema Weight loss Hernia Anemia Hepatic failure Bruising susceptibility Nystagmus Recurrent pharyngitis Renal tubular acidosis Glycosuria Abnormality of lipid metabolism Celiac disease Xerostomia Orthostatic hypotension Wheezing Abnormal EKG Interstitial pulmonary abnormality Hypertrophic cardiomyopathy Hypohidrosis Renal tubular dysfunction Clubbing of fingers High-frequency hearing impairment Restrictive cardiomyopathy Abnormality of the nose Abnormality of femur morphology Chronic fatigue Myocardial fibrosis Sinus bradycardia Achalasia Chronic obstructive pulmonary disease Angina pectoris Proteinuria Edema of the lower limbs Abnormality of the nervous system Peripheral arterial stenosis Reduced ejection fraction Heat intolerance Supraventricular tachycardia Large earlobe Abnormality of the gastrointestinal tract Tubular atrophy Elevated serum creatinine Tubulointerstitial nephritis Oligospermia Anhidrosis Abnormality of the kidney Syncope Reduced bone mineral density Thick vermilion border Ischemic stroke Corneal dystrophy Ventricular tachycardia Hyperlipidemia Aminoaciduria Exercise intolerance Nephropathy Muscle cramps Spontaneous abortion Urinary incontinence Thick eyebrow Hypotension Abnormality of the cardiovascular system Ventricular hypertrophy Thick lower lip vermilion Atrial fibrillation Abnormal autonomic nervous system physiology Abnormal mitral valve morphology Palpitations Fasciculations Left ventricular hypertrophy Bradycardia Ventricular arrhythmia Bulbous nose Prominent nasal bridge Clubbing Coronary artery atherosclerosis Impotence Bundle branch block Loss of consciousness Corneal opacity Emphysema Lymphedema Polyuria Pruritus Tricuspid regurgitation Impaired vibratory sensation Heart murmur Easy fatigability Personality changes Polydipsia Abnormality of the cerebral white matter Glomerulosclerosis Hemiplegia Delayed puberty Abnormality of the hand Prominent supraorbital ridges Chronic kidney disease Atrioventricular block Stage 5 chronic kidney disease Tachycardia Asymmetric septal hypertrophy Heavy proteinuria Periorbital fullness Pectus carinatum High myopia Limb undergrowth Waddling gait Retinal detachment Pulmonary hypoplasia Retinal degeneration Micromelia Genu valgum Narrow chest Platyspondyly Broad forehead Respiratory tract infection Abnormality of the metaphysis Hyperlordosis Skeletal dysplasia Polydactyly Severe short stature Malar flattening Kyphosis Respiratory distress Short neck Myopia Cleft palate Muscular hypotonia Lumbar hyperlordosis Abnormal form of the vertebral bodies Abnormal glomerular filtration rate Barrel-shaped chest Limitation of knee mobility Neonatal short-trunk short stature Sciatica Delayed pubic bone ossification Retinoschisis Limited hip movement Cervical myelopathy Flattened epiphysis Limited elbow movement Myelopathy Ovoid vertebral bodies Vitreoretinopathy Abnormality of epiphysis morphology Hypoplasia of the odontoid process Disproportionate short stature Restrictive ventilatory defect Short thorax Vestibular dysfunction Bowing of the legs Spondyloepiphyseal dysplasia Back pain Genu varum Growth abnormality Coxa vara Rhizomelia Cornea verticillata Abnormality of the common coagulation pathway Abnormal aortic valve morphology Biventricular hypertrophy Vascular tortuosity Decreased glomerular filtration rate Nephrogenic diabetes insipidus Abnormality of temperature regulation Limb pain Corneal crystals Retinal vascular tortuosity Vascular skin abnormality Decreased female libido Abnormality of cardiovascular system physiology Abnormal endocardium morphology Primary hypothyroidism Increased blood urea nitrogen Microalbuminuria Conjunctival telangiectasia Supraventricular arrhythmia Dysesthesia Abnormal cornea morphology Abnormality of the renal tubule Abnormal thrombosis Tubulointerstitial fibrosis Chronic pain Abnormal renal physiology Miosis T-wave inversion Distal renal tubular acidosis Reduced sperm motility Increased glomerular filtration rate Impaired renal concentrating ability Increased carotid artery intimal medial thickness Abnormal ST segment Abnormal common carotid artery morphology Acroparesthesia Carcinoma Tenesmus Left ventricular septal hypertrophy Tortuosity of conjunctival vessels Hyperkeratotic papule Abnormality of the forehead Abnormality of glycosphingolipid metabolism Functional abnormality of the gastrointestinal tract Angiokeratoma ST segment depression Unexplained fevers Mucosal telangiectasiae Concentric hypertrophic cardiomyopathy Coronary artery stenosis Shortened PR interval Decreased lacrimation Angiokeratoma corporis diffusum Shortened QT interval Hyposthenuria Impaired temperature sensation Obstructive lung disease Anxiety Telangiectasia Coarse facial features Eczema Increased IgA level Large forehead Posterior subcapsular cataract Poor coordination Peripheral visual field loss Subcapsular cataract Colitis Apathy Recurrent pneumonia Long eyelashes Dehydration Neutrophilia Aciduria Sepsis Retinal dystrophy Infertility Nyctalopia Pallor Postnatal growth retardation Hepatosplenomegaly Rod-cone dystrophy Pneumonia Porokeratosis Serositis Hepatomegaly Venous thrombosis Pustule Aseptic necrosis Pulmonary embolism Blurred vision Epiphora Inflammation of the large intestine Acne Pleural effusion Encephalitis Increased intracranial pressure Pancreatitis Pharyngitis Hemiparesis Abnormal blistering of the skin Memory impairment Confusion Abnormal pyramidal sign Retinopathy Scarring Irritability Photophobia Reduced visual acuity Hyperreflexia Frontal bossing Failure to thrive Raynaud phenomenon Epistaxis Impaired mastication Abdominal aortic aneurysm Amaurosis fugax Mediastinal lymphadenopathy Abnormality of the pleura Abnormal thrombocyte morphology Visual field defect Ophthalmoparesis Skin ulcer Diplopia Conductive hearing impairment Arteritis Visual impairment Fasciitis Hepatic amyloidosis Abnormality of the sacroiliac joint Conjunctival hyperemia Lymphocytosis Elevated C-reactive protein level Reticulocytosis Cellulitis Muscle stiffness Peripheral demyelination Glossitis Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis Microcephaly Decreased fertility Genital hernia Tendon rupture Premature rupture of membranes Anorectal anomaly Abnormality of the menstrual cycle Venous insufficiency Abnormality of the wrist Atypical scarring of skin Soft skin Striae distensae Elbow dislocation Retinal arteritis Hyperextensible skin Decreased nerve conduction velocity Abnormal palate morphology Wormian bones Sleep disturbance Abnormality of the foot Joint laxity Pes planus Gastroesophageal reflux Osteoporosis Jaw claudication Pulmonary infiltrates Stomatitis Mandibular prognathia Reduced consciousness/confusion Dermal translucency Excessive wrinkled skin Abnormality of hair texture Ocular pain Arterial stenosis Premature loss of primary teeth Pneumothorax Bladder diverticulum Abnormal pupil morphology Aplasia/Hypoplasia of the earlobes Osteolytic defects of the phalanges of the hand Colonic diverticula Varicose veins Hematochezia Abnormally large globe Periodontitis Narrow nose Abnormal eyelash morphology Subarachnoid hemorrhage Dilatation of the cerebral artery Alopecia of scalp Premature loss of teeth Abnormal oral frenulum morphology Internal hemorrhage Esophageal atresia Uterine rupture Hypothyroidism Hyperkeratosis Posteriorly rotated ears Cardiomyopathy Hypermobility of distal interphalangeal joints Hemothorax Premature delivery because of cervical insufficiency or membrane fragility Hypoplastic lacrimal duct Arteriovenous fistulas of celiac and mesenteric vessels Uterine prolapse Arterial rupture Cigarette-paper scars Foot acroosteolysis Spontaneous pneumothorax Molluscoid pseudotumors Coronary artery aneurysm Gingival recession Pulmonary artery aneurysm Normal pressure hydrocephalus Peripheral arteriovenous fistula Renovascular hypertension Absent earlobe Arteriovenous fistula Sprengel anomaly Prematurely aged appearance Alopecia areata Superficial thrombophlebitis Hypospadias Abnormality of cardiovascular system morphology Hydrocephalus Macrocephaly Cryptorchidism Hypopyon Decreased level of D-mannose in urine Epididymitis Genital ulcers Panuveitis Retrobulbar optic neuritis Narrow mouth Iritis Increased inflammatory response Iridocyclitis Posterior uveitis Anterior uveitis Chorioretinitis Immunologic hypersensitivity Erythema nodosum Thrombophlebitis Oral ulcer Endocarditis Pectus excavatum Proptosis Scleroderma Congenital hip dislocation Abnormal joint morphology Fragile skin Narrow nasal bridge Aplasia/Hypoplasia of the eyebrow Melanocytic nevus Aortic aneurysm Redundant skin Hypokalemia Abnormality of the urinary system Short chin Cardiac arrest Deeply set eye Abnormality of the face Blue sclerae Abnormality of the skin Premature birth Abnormal bleeding High, narrow palate Thin vermilion border Abnormality of skin pigmentation Carious teeth Protruding ear Telecanthus Delayed calcaneal ossification



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