Arthritis, and Dysphagia

Diseases related with Arthritis and Dysphagia

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


Top matches:

Low match PERIPHERAL NEUROPATHY-MYOPATHY-HOARSENESS-HEARING LOSS SYNDROME


Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome is a rare, syndromic genetic deafness characterized by a combination of muscle weakness, chronic neuropathic and myopathic features, hoarseness and sensorineural hearing loss. A wide range of disease onset and severity has been reported even within the same family.

PERIPHERAL NEUROPATHY-MYOPATHY-HOARSENESS-HEARING LOSS SYNDROME Is also known as peripheral neuropathy-myopathy-hoarseness-deafness syndrome

Related symptoms:

  • Hearing impairment
  • Sensorineural hearing impairment
  • Muscle weakness
  • Peripheral neuropathy
  • Tremor


SOURCES: OMIM ORPHANET MENDELIAN

More info about PERIPHERAL NEUROPATHY-MYOPATHY-HOARSENESS-HEARING LOSS SYNDROME

Low match IDIOPATHIC ACHALASIA


Idiopathic achalasia (IA) is a primary esophageal motor disorder characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter (LES) relaxation in response to deglutition.

IDIOPATHIC ACHALASIA Is also known as idiopathic achalasia of esophagus|achalasia cardia|primary achalasia

Related symptoms:

  • Pain
  • Dysphagia
  • Vomiting
  • Weight loss
  • Gastroesophageal reflux


SOURCES: ORPHANET OMIM MENDELIAN

More info about IDIOPATHIC ACHALASIA

Low match DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS


Diffuse cutaneous systemic sclerosis (dcSSc) is a subtype of Systemic Sclerosis (SSc; see this term) characterized by truncal and acral skin fibrosis with an early and significant incidence of diffuse involvement (interstitial lung disease, oliguric renal failure, diffuse gastrointestinal disease, and myocardial involvement).

DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS Is also known as progressive cutaneous systemic scleroderma|diffuse cutaneous systemic scleroderma|progressive cutaneous systemic sclerosis

Related symptoms:

  • Muscle weakness
  • Pain
  • Flexion contracture
  • Hypertension
  • Dysphagia


SOURCES: ORPHANET MENDELIAN

More info about DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS

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Other less relevant matches:

Low match REYNOLDS SYNDROME


Reynolds syndrome (RS) is an autoimmune disorder characterized by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc) (see these terms).

REYNOLDS SYNDROME Is also known as primary biliary cirrhosis and systemic scleroderma|primary biliary cirrhosis, scleroderma, raynaud disease, and telangiectasia

Related symptoms:

  • Pain
  • Hepatomegaly
  • Fever
  • Fatigue
  • Dysphagia


SOURCES: OMIM ORPHANET MENDELIAN

More info about REYNOLDS SYNDROME

Low match MULTIPLE SYMMETRIC LIPOMATOSIS


Multiple symmetric lipomatosis (MSL) is a rare subcutaneous tissue disease characterized by growth of symmetric non-encapsulated masses of adipose tissue mostly around the face and neck with variable clinical repercussions (e.g. reduced neck mobility, compression of respiratory structures).

MULTIPLE SYMMETRIC LIPOMATOSIS Is also known as launois-bensaude lipomatosis|familial benign cervical lipomatosis|madelung disease|cephalothoracic lipodystrophy|lipomatosis, familial benign cervical|lipodystrophy, cephalothoracic

Related symptoms:

  • Neoplasm
  • Pain
  • Anemia
  • Hypertension
  • Peripheral neuropathy


SOURCES: ORPHANET OMIM MENDELIAN

More info about MULTIPLE SYMMETRIC LIPOMATOSIS

Low match LESCH-NYHAN SYNDROME; LNS


LESCH-NYHAN SYNDROME; LNS Is also known as hprt deficiency, complete|hypoxanthine guanine phosphoribosyltransferase 1 deficiency|hprt deficiency|hprt1 deficiency

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Scoliosis


SOURCES: OMIM MENDELIAN

More info about LESCH-NYHAN SYNDROME; LNS

Low match PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3


Proteasome-associated autoinflammatory syndrome-3 is an autosomal recessive syndrome with onset in early infancy. Affected individuals present with nodular dermatitis, recurrent fever, myositis, panniculitis-induced lipodystrophy, lymphadenopathy, and dysregulation of the immune response, particularly associated with abnormal type I interferon-induced gene expression patterns. Additional features are highly variable, but may include joint contractures, hepatosplenomegaly, anemia, thrombocytopenia, recurrent infections, autoantibodies, and hypergammaglobulinemia. Some patients may have intracranial calcifications (summary by Brehm et al., 2015).For a discussion of genetic heterogeneity of PRAAS, see PRAAS1 (OMIM ).

Related symptoms:

  • Failure to thrive
  • Anemia
  • Flexion contracture
  • Fever
  • Dysphagia


SOURCES: OMIM MENDELIAN

More info about PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3

Low match JUVENILE HUNTINGTON DISEASE


Juvenile Huntington disease (JHD) is a form of Huntington disease (HD; see this term), characterized by onset of signs and symptoms before 20 years of age.

JUVENILE HUNTINGTON DISEASE Is also known as huntington chorea|jhd|juvenile huntington chorea

Related symptoms:

  • Seizures
  • Ataxia
  • Cognitive impairment
  • Anemia
  • Delayed speech and language development


SOURCES: OMIM ORPHANET MENDELIAN

More info about JUVENILE HUNTINGTON DISEASE

Low match LETHAL ATAXIA WITH DEAFNESS AND OPTIC ATROPHY


Lethal ataxia with deafness and optic atrophy (also known as Arts syndrome) is characterized by intellectual deficit, early-onset hypotonia, ataxia, delayed motor development, hearing impairment and loss of vision due to optic atrophy.

LETHAL ATAXIA WITH DEAFNESS AND OPTIC ATROPHY Is also known as mrxsarts|arts syndrome|mental retardation, x-linked, syndromic, arts type|mrxs18|mental retardation, x-linked, syndromic 18|ataxia, fatal x-linked, with deafness and loss of vision

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about LETHAL ATAXIA WITH DEAFNESS AND OPTIC ATROPHY

Low match EHLERS-DANLOS SYNDROME TYPE 7B


Arthrochalasia-type EDS is distinguished from other types of EDS by the frequency of congenital hip dislocation and extreme joint laxity with recurrent joint subluxations and minimal skin involvement (Byers et al., 1997; Giunta et al., 2008).For a discussion of genetic heterogeneity of arthrochalasia-type EDS, see {130060}.

EHLERS-DANLOS SYNDROME TYPE 7B Is also known as eds viib|ehlers-danlos syndrome, type viib, autosomal dominant|eds7b

Related symptoms:

  • Short stature
  • Generalized hypotonia
  • Scoliosis
  • Micrognathia
  • Muscle weakness


SOURCES: OMIM ORPHANET MENDELIAN

More info about EHLERS-DANLOS SYNDROME TYPE 7B

Top 5 symptoms//phenotypes associated to Arthritis and Dysphagia

Symptoms // Phenotype % cases
Pain Uncommon - Between 30% and 50% cases
Anemia Uncommon - Between 30% and 50% cases
Gastroesophageal reflux Uncommon - Between 30% and 50% cases
Xerostomia Uncommon - Between 30% and 50% cases
Oral-pharyngeal dysphagia Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Flexion contracture Hypertension Gout Weight loss Vomiting Arthralgia Generalized hypotonia Hoarse voice Aggressive behavior Hyperreflexia Peripheral neuropathy Muscle weakness

Rare Symptoms - Less than 30% cases


Scoliosis Short stature Global developmental delay Scleroderma Sensorineural hearing impairment Clumsiness Telangiectasia of the skin Intellectual disability Muscular hypotonia Hepatomegaly Delayed speech and language development Fever Chorea Respiratory insufficiency Calcinosis Telangiectasia Elevated hepatic transaminase Hip dislocation Abnormality of the liver Skin rash Irritability Rigidity Motor delay Intellectual disability, mild Dystonia Skin ulcer Hearing impairment Behavioral abnormality Babinski sign Tremor Areflexia Hyporeflexia Pneumonia Recurrent infections Cough Rheumatoid arthritis Abnormality of the skin Keratoconjunctivitis sicca Diabetes mellitus Testicular atrophy Gait disturbance Renal insufficiency Cognitive impairment Dysarthria Seizures Ataxia Involuntary movements Progressive cerebellar ataxia Hyperkinesis Brain atrophy Schizophrenia Progressive neurologic deterioration Broad-based gait Abnormal cerebellum morphology Type II diabetes mellitus Generalized-onset seizure Neuronal loss in central nervous system Bradykinesia Gliosis Gait ataxia Neurodegeneration Finger swelling Conjunctivitis Hypercholesterolemia Lipodystrophy Keratitis Increased antibody level in blood Hypermelanotic macule Microcytic anemia Myositis Bronchiolitis Hypochromic anemia Panniculitis Bronchiolitis obliterans Bronchiolitis obliterans organizing pneumonia Falls Ventriculomegaly Cerebellar atrophy Depressivity Dementia Myoclonus Hyperactivity Slurred speech Anxiety Mental deterioration Abnormality of the cerebral white matter Abnormality of eye movement Infertility Abnormality of movement Incoordination Abnormal involuntary eye movements Personality changes Kyphosis Hyperlordosis Joint laxity Pes planus Umbilical hernia Osteoporosis Hernia Talipes equinovarus Joint hypermobility Depressed nasal bridge Micrognathia Spinal cord posterior columns myelin loss Parietal cortical atrophy Increased urinary hypoxanthine Muscle mounding Joint hyperflexibility Bruising susceptibility Low frustration tolerance Hallux valgus Excessive wrinkled skin Poor wound healing Hyperextensibility of the finger joints Soft skin Fragile skin Atrophic scars Hyperextensible skin Recurrent fractures Delayed gross motor development Joint dislocation Wormian bones Congenital hip dislocation Osteoarthritis Blue sclerae Pancreatic fibrosis Arnold-Chiari type I malformation Obsessive-compulsive behavior Head tremor Neuronal loss in basal ganglia Sinusitis Mania Paranoia Dilated fourth ventricle Chronic bronchitis Upper limb undergrowth Frequent temper tantrums Restlessness Cerebellar vermis atrophy Bronchitis Muscle fibrillation Hypokinesia Akinesia Suicidal ideation Oral motor hypotonia Decreased nerve conduction velocity Neonatal hypotonia Recurrent upper respiratory tract infections Drooling Sensorimotor neuropathy Progressive muscle weakness Progressive visual loss Tetraplegia Cerebral cortical atrophy Growth delay Elevated serum creatine phosphokinase Visual loss Absent speech Immunodeficiency Optic atrophy Visual impairment Nystagmus Lymphopenia Recurrent urinary tract infections Inflammatory abnormality of the skin Elevated alkaline phosphatase Abnormal bowel sounds Fatigue Splenomegaly Jaundice Myalgia Pruritus Cirrhosis Ascites Gastrointestinal hemorrhage Cholestasis Hyperbilirubinemia Encephalitis Steatorrhea Hypertensive crisis Elevated erythrocyte sedimentation rate Irregular hyperpigmentation Raynaud phenomenon Antinuclear antibody positivity Esophageal varix Biliary cirrhosis Lichenification Abnormality of the gastric mucosa Mucosal telangiectasiae Sclerodactyly Lip telangiectasia Palmar telangiectasia Narrow foramen obturatorium Decreased urine output Generalized abnormality of skin Keratoconjunctivitis Myopathy Distal muscle weakness Abnormality of the foot Distal amyotrophy Mildly elevated creatine phosphokinase Progressive peripheral neuropathy Vocal cord paresis Chest pain Asthma Aspiration Adrenal insufficiency Achalasia Diarrhea Dyspareunia Congestive heart failure Constipation Dyspnea Autoimmunity Carious teeth Malabsorption Nausea and vomiting Pulmonary arterial hypertension Osteolysis Pulmonary fibrosis Pulmonary infiltrates Osteolytic defects of the phalanges of the hand Oliguria Calcinosis cutis Neoplasm Hypertriglyceridemia Megaloblastic anemia Choreoathetosis Nephrolithiasis Stereotypy Spastic gait Finger clinodactyly Cerebral palsy Self-injurious behavior Proximal placement of thumb Athetosis Opisthotonus Hyperuricemia Self-mutilation Dyslexia Nephropathy Focal dystonia Facial grimacing Hyperuricosuria Excessive purine production Bladder stones Podagra Failure to thrive Thrombocytopenia Hepatosplenomegaly Erythema Scarring Lymphadenopathy Cerebral calcification Abnormality of extrapyramidal motor function Hematuria Pes cavus Axonal degeneration Hypothyroidism Joint stiffness Paresthesia Tachycardia Polyneuropathy Muscle cramps Myocardial infarction Insulin resistance Reduced tendon reflexes Ragged-red muscle fibers Abnormality of mitochondrial metabolism Coronary artery atherosclerosis Multiple lipomas Clinodactyly of the 5th finger Arthropathy Macrocytic anemia Lipoma Oligomenorrhea Hyperlipoproteinemia Alcoholism Decreased LDL cholesterol concentration Neuropathic arthropathy Increased HDL cholesterol concentration Abnormal adipose tissue morphology Spasticity Hypertonia Clinodactyly Subcutaneous hemorrhage



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