Arthritis, and Migraine

Diseases related with Arthritis and Migraine

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


Top matches:

Medium 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

Medium match TAKAYASU ARTERITIS


Takayasu arteritis (TAK) is a rare inflammatory large-vessel vasculitis primarily affecting the aorta and its major branches, but also other large vessels, causing stenosis, occlusion, or aneurysm.

TAKAYASU ARTERITIS Is also known as young female arteritis|aortic arch syndrome|pulseless disease

Related symptoms:

  • Seizures
  • Muscle weakness
  • Anemia
  • Hypertension
  • Fever


SOURCES: ORPHANET OMIM MENDELIAN

More info about TAKAYASU ARTERITIS

Low match CINCA SYNDROME


Chronic Infantile Neurological, Cutaneous, and Articular (CINCA) syndrome is characterised by skin rash, joint involvement, chronic meningitis with granulocytes and, in some cases, sensorineural hearing loss and ocular signs.

CINCA SYNDROME Is also known as multisystem inflammatory disease, neonatal-onset|nomid syndrome|iomid syndrome|infantile-onset multisystem inflammatory disease|prieur-griscelli syndrome|neonatal-onset multisystem inflammatory disease|chronic neurologic cutaneous and articular syndrome|c

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Hearing impairment
  • Growth delay
  • Sensorineural hearing impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about CINCA SYNDROME

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Other less relevant matches:

Low match ANEURYSM-OSTEOARTHRITIS SYNDROME


ANEURYSM-OSTEOARTHRITIS SYNDROME Is also known as loeys-dietz syndrome with osteoarthritis|loeys-dietz syndrome, type 1c, formerly|lds1c, formerly|aneurysms-osteoarthritis syndrome

Related symptoms:

  • Scoliosis
  • Hypertelorism
  • Cleft palate
  • Pain
  • High palate


SOURCES: ORPHANET OMIM MENDELIAN

More info about ANEURYSM-OSTEOARTHRITIS SYNDROME

Low match ATTRV30M AMYLOIDOSIS


Familial amyloid polyneuropathy (FAP) or transthyretin (TTR) amyloid polyneuropathy is a progressive sensorimotor and autonomic neuropathy of adulthood onset. Weight loss and cardiac involvement are frequent; ocular or renal complications may also occur.

ATTRV30M AMYLOIDOSIS Is also known as familial amyloid polyneuropathy type i|ttr amyloid neuropathy|attrv30m-related amyloidosis|hereditary amyloidosis, transthyretin-related|transthyretin amyloid polyneuropathy|familial amyloid polyneuropathy, portuguese-swedish-japanese type|fap|amyloid pol

Related symptoms:

  • Seizures
  • Hearing impairment
  • Ataxia
  • Nystagmus
  • Sensorineural hearing impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about ATTRV30M AMYLOIDOSIS

Low match KAWASAKI DISEASE


Kawasaki disease (KD) is a febrile, systemic, self-limiting vasculitis affecting children and characterized by inflammation in the medium sized vessels associated with coronary arterial aneurysms (CAA) that may be life threatening when untreated. KD is the most common cause of acquired heart disease in children in developed countries and is a risk factor for ischemic heart disease in adulthood.

KAWASAKI DISEASE Is also known as kd|infantile polyarteritis|mucocutaneous lymph node syndrome

Related symptoms:

  • Sensorineural hearing impairment
  • Ptosis
  • Fever
  • Fatigue
  • Edema


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about KAWASAKI DISEASE

Low 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

Low match ACROMEGALY


Acromegaly is an acquired disorder related to excessive production of growth hormone (GH) and characterized by progressive somatic disfigurement (mainly involving the face and extremities) and systemic manifestations.

Related symptoms:

  • Neoplasm
  • Hypertension
  • Fatigue
  • Frontal bossing
  • Abnormality of the dentition


SOURCES: ORPHANET MENDELIAN

More info about ACROMEGALY

Low 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

Low 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

Top 5 symptoms//phenotypes associated to Arthritis and Migraine

Symptoms // Phenotype % cases
Arthralgia Common - Between 50% and 80% cases
Fever Common - Between 50% and 80% cases
Fatigue Common - Between 50% and 80% cases
Headache Common - Between 50% and 80% cases
Vasculitis Common - Between 50% and 80% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Lymphadenopathy Myalgia Pain Paresthesia Skin rash Leukocytosis Elevated erythrocyte sedimentation rate Amyloidosis Dilatation Sensorineural hearing impairment Constipation Vomiting Edema Conjunctivitis Diarrhea Inguinal hernia Frontal bossing Splenomegaly Papule Nausea and vomiting Meningitis Erythema Arrhythmia Osteoarthritis Uveitis Elevated C-reactive protein level Abdominal pain Depressivity Scoliosis Mitral regurgitation Inflammatory abnormality of the eye Ascending tubular aorta aneurysm Hearing impairment Neoplasm Urticaria Nausea Vertigo Cervical lymphadenopathy Seizures Anemia Hyperhidrosis

Rare Symptoms - Less than 30% cases


Weight loss Hypertension Abnormal myocardium morphology Hernia Recurrent pharyngitis Hypertelorism Hypertrophic cardiomyopathy Umbilical hernia Ptosis Chest pain Abnormality of the dentition Osteoporosis Bruising susceptibility Pes planus Joint laxity Subcutaneous nodule Mitral valve prolapse Acrocyanosis Muscle weakness Striae distensae Soft skin Impotence Limitation of joint mobility Abdominal distention Ataxia Peripheral demyelination Congestive heart failure Renal insufficiency Myocardial infarction Abnormal joint morphology Malabsorption Abnormal heart valve morphology Growth delay Intellectual disability Pericarditis Peritonitis Visual impairment Hepatomegaly Arteritis Hypermelanotic macule Blindness Chills Hepatosplenomegaly Neuritis Aortic root aneurysm Intestinal obstruction Global developmental delay Aortic regurgitation Episodic fever Optic neuritis Joint dislocation Erysipelas Cranial nerve paralysis Conjunctival hyperemia Purpura Abnormal gallbladder morphology Deep palmar crease Anterior hypopituitarism Cerebral palsy Sleep apnea Growth abnormality Acne Large hands Generalized hyperpigmentation Spinal canal stenosis Reticulocytosis Palpebral edema Joint swelling Neoplasm of the endocrine system Cellulitis Growth hormone excess Broad foot Abnormal toenail morphology Widely spaced teeth Abnormality of the endocrine system Dysuria Macule Myositis Thick lower lip vermilion Acanthosis nigricans Broad forehead Abnormality of the sacroiliac joint Hepatic amyloidosis Fasciitis Kyphosis Behavioral abnormality Diabetes mellitus Hepatic failure Mandibular prognathia Macrotia Muscle stiffness Pleuritis Anxiety Synophrys Abnormality of the fingernails Long face Lymphocytosis Periorbital edema Wide nose Tapered finger Macroglossia Full cheeks Orchitis Tall stature Thickened skin Hoarse voice Generalized hirsutism Coarse facial features Decreased nerve conduction velocity Pheochromocytoma Pneumonia Retinal dystrophy Infertility Cough Nyctalopia Pallor Postnatal growth retardation Rod-cone dystrophy Flexion contracture Gastrointestinal hemorrhage Cataract Failure to thrive Microcephaly Generalized hypotonia Genital hernia Cystocele Tendon rupture Sepsis Aciduria Arterial dissection Poor coordination Serositis Neutrophilia Porokeratosis Increased IgA level Recurrent aphthous stomatitis Large forehead Posterior subcapsular cataract Peripheral visual field loss Dehydration Subcapsular cataract Colitis Apathy Recurrent pneumonia Long eyelashes Nephrotic syndrome Optic disc pallor Eczema Premature rupture of membranes Anorectal anomaly Long penis Abnormality of reproductive system physiology Joint hyperflexibility Abnormality of the foot Hip dislocation Apnea Gastroesophageal reflux Epicanthus Cortical diaphyseal thickening of the upper limbs Broad jaw Sleep disturbance Macrodactyly Dysmenorrhea Pituitary prolactin cell adenoma Deep plantar creases Galactorrhea Hypersomnia Paraganglioma Joint hypermobility Microdontia Abnormality of the gingiva Keratoconjunctivitis sicca Abnormality of the menstrual cycle Venous insufficiency Gastrointestinal dysmotility Aplasia/Hypoplasia of the abdominal wall musculature Abnormality of the wrist Atypical scarring of skin Gingivitis Keratoconus Thin skin Decreased fertility Elbow dislocation Hyperextensible skin Strawberry tongue Abnormal palate morphology Osteolysis Wormian bones Gingival overgrowth Aseptic leukocyturia Orthostatic hypotension due to autonomic dysfunction Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis Ventricular hypertrophy Disproportionate tall stature Aortic aneurysm Back pain Bicuspid aortic valve Left ventricular hypertrophy Atrial fibrillation Dental malocclusion Slender finger Arachnodactyly Pulmonic stenosis Camptodactyly Patent ductus arteriosus Atrial septal defect Abnormality of the skeletal system High palate Abnormality of the sternum Subarachnoid hemorrhage Abnormal granulocyte morphology Abdominal aortic aneurysm Spasticity Nystagmus Knee osteoarthritis Uterine prolapse Intervertebral disc degeneration Protrusio acetabuli Dural ectasia Dilatation of the cerebral artery Arterial tortuosity Hip osteoarthritis Thoracic aortic aneurysm Osteochondritis Dissecans Low back pain Spondylolisthesis Aortic dissection Cleft palate Retrobulbar optic neuritis Dysarthria Gangrene Abnormal endocardium morphology Arterial stenosis Abnormal pattern of respiration Abnormal aortic valve morphology Reduced consciousness/confusion Cerebral ischemia Hemoptysis Gastrointestinal infarctions Psoriasiform dermatitis Skin ulcer Anorexia Pulmonary arterial hypertension Neurological speech impairment Retinopathy Progressive hearing impairment Amaurosis fugax Hypertensive crisis Pseudopapilledema Increased intracranial pressure Abnormality of neutrophils Delayed closure of the anterior fontanelle Abnormal thrombocyte morphology Juvenile rheumatoid arthritis Arthropathy Progressive sensorineural hearing impairment Reduced bone mineral density Overgrowth Increased inflammatory response Premature birth EEG abnormality Skeletal dysplasia Proptosis Macrocephaly Brachydactyly Abnormal facial shape Peripheral neuropathy Tremor Abnormal emotion/affect behavior Respiratory tract infection Hypoalbuminemia Ischemic stroke Decreased liver function Cholestasis Hepatitis Hematuria Irritability Hyponatremia Proteinuria Jaundice Amyloid deposition in the vitreous humor Cardiac amyloidosis Vitreous floaters Psychomotor deterioration Urinary retention Scaling skin Coronary artery atherosclerosis Abnormal renal physiology Glossitis Pyuria Arthralgia/arthritis Abnormality of nail color Coronary artery aneurysm CSF pleocytosis Abnormal pericardium morphology Abnormal oral mucosa morphology Interstitial pulmonary abnormality Cholecystitis Synovitis Cheilitis Allergy Myocarditis Tubulointerstitial nephritis Acute kidney injury Sensory ataxia Myelopathy Hydrocephalus Polyneuropathy Bilateral sensorineural hearing impairment Neuronal loss in central nervous system Hypotension Urinary incontinence Gliosis Coma Nephropathy Hemiparesis Peripheral axonal neuropathy Paraplegia Facial palsy Dementia Hyporeflexia Areflexia Cardiomyopathy Cardiomegaly Hallucinations Constrictive median neuropathy Axonal degeneration Stroke-like episode Multiple myeloma Restrictive cardiomyopathy Increased CSF protein Syringomyelia Decreased number of peripheral myelinated nerve fibers Orthostatic hypotension Aphasia Abnormal autonomic nervous system physiology Malnutrition Cerebral hemorrhage Rheumatoid arthritis Cachexia Atrioventricular block Spastic paraparesis Paraparesis Pharyngitis



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