Arthritis, and Nausea and vomiting

Diseases related with Arthritis and Nausea and vomiting

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


Top matches:

Low match FAMILIAL COLD URTICARIA


Familial cold urticaria (FCAS) is the mildest form of cryopyrin-associated periodic syndrome (CAPS; see this term) and is characterized by recurrent episodes of urticaria-like skin rash triggered by exposure to cold associated with low-grade fever, general malaise, eye redness and arthralgia/myalgia.

FAMILIAL COLD URTICARIA Is also known as fcas|familial cold autoinflammatory syndrome|fcu

Related symptoms:

  • Sensorineural hearing impairment
  • Fever
  • Fatigue
  • Headache
  • Hyperhidrosis


SOURCES: ORPHANET MENDELIAN

More info about FAMILIAL COLD URTICARIA

Low match IMMUNODEFICIENCY 57; IMD57


Related symptoms:

  • Failure to thrive
  • Vomiting
  • Diarrhea
  • Immunodeficiency
  • Recurrent infections


SOURCES: OMIM MENDELIAN

More info about IMMUNODEFICIENCY 57; IMD57

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

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Other less relevant matches:

Low match GENERALIZED PUSTULAR PSORIASIS


Generalized pustular psoriasis is a severe inflammatory skin disease that can be life-threatening and that is characterized by recurrent episodes of high fever, fatigue, episodic erythematous cutaneous eruptions with sterile cutaneous pustules formation on various parts of the body, and neutrophil leukocytosis.

GENERALIZED PUSTULAR PSORIASIS Is also known as ditra|interleukin 36 receptor antagonist deficiency|acrodermatitis continua of hallopeau|generalized pustular psoriasis|psorp|gpp|palmoplantar pustulosis

Related symptoms:

  • Muscle weakness
  • Fever
  • Headache
  • Erythema
  • Skin rash


SOURCES: OMIM ORPHANET MENDELIAN

More info about GENERALIZED PUSTULAR PSORIASIS

Low match NLRP12-ASSOCIATED HEREDITARY PERIODIC FEVER SYNDROME


NLRP12-associated hereditary periodic fever syndrome is a rare autoinflammatory syndrome characterized by episodic and recurrent periods of fever combined with various systemic manifestations such as myalgia, arthralgia, joint swelling, urticaria, headache and skin rash. Common trigger of these episodes is cold.

NLRP12-ASSOCIATED HEREDITARY PERIODIC FEVER SYNDROME Is also known as familial cold autoinflammatory syndrome type 2|naps12|fcas2

Related symptoms:

  • Intellectual disability
  • Hearing impairment
  • Sensorineural hearing impairment
  • Pain
  • Fever


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about NLRP12-ASSOCIATED HEREDITARY PERIODIC FEVER SYNDROME

Low match PERIODIC FEVER-INFANTILE ENTEROCOLITIS-AUTOINFLAMMATORY SYNDROME


Autoinflammation with infantile enterocolitis is an autosomal dominant disorder characterized by onset of recurrent flares of autoinflammation in early infancy. Affected individuals tend to have poor overall growth and gastrointestinal symptoms in infancy associated with laboratory evidence of activated inflammation. This initial presentation is followed by recurrent febrile episodes with splenomegaly and sometimes hematologic disturbances, arthralgias, or myalgias. The disorder results from overactivation of an arm of the immune response system (Romberg et al., 2014; Canna et al., 2014).

PERIODIC FEVER-INFANTILE ENTEROCOLITIS-AUTOINFLAMMATORY SYNDROME Is also known as nlrc4-related macrophage activation syndrome|nlrc4-related infantile enterocolitis-autoinflammatory syndrome|nlrc4-related autoinflammatory syndrome with macrophage activation syndrome|nlrc4-related mas|nlrc4-related autoinflammatory syndrome with mas

Related symptoms:

  • Seizures
  • Short stature
  • Failure to thrive
  • Pain
  • Anemia


SOURCES: OMIM ORPHANET MENDELIAN

More info about PERIODIC FEVER-INFANTILE ENTEROCOLITIS-AUTOINFLAMMATORY SYNDROME

Low match COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH


Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia is an inborn error of folate metabolism due to deficiency of methylenetetrahydrofolate dehydrogenase-1. Manifestations may include hemolytic uremic syndrome, macrocytosis, epilepsy, hearing loss, retinopathy, mild mental retardation, lymphopenia involving all subsets, and low T-cell receptor excision circles. Folinic acid supplementation is an effective treatment (summary by Ramakrishnan et al., 2016).

COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH Is also known as methylenetetrahydrofolate dehydrogenase 1 deficiency

Related symptoms:

  • Intellectual disability
  • Seizures
  • Hearing impairment
  • Sensorineural hearing impairment
  • Anemia


SOURCES: OMIM MENDELIAN

More info about COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH

Low match CATARACT-GLAUCOMA SYNDROME


Cataract-glaucoma syndrome is characterised by the association of total bilateral congenital cataract with the secondary occurrence of glaucoma appearing at ages varying between 10 and 40 years.

Related symptoms:

  • Seizures
  • Short stature
  • Generalized hypotonia
  • Pain
  • Feeding difficulties


SOURCES: ORPHANET MENDELIAN

More info about CATARACT-GLAUCOMA SYNDROME

Low match PARASTREMMATIC DWARFISM


Parastremmatic dwarfism is a very rare chondrodysplasia characterized by severe dwarfism, kyphoscoliosis, stiffness of large joints and distortion of lower limbs.

Related symptoms:

  • Short stature
  • Scoliosis
  • Flexion contracture
  • Brachydactyly
  • Short neck


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about PARASTREMMATIC DWARFISM

Low match GLYCOGEN STORAGE DISEASE DUE TO GLYCOGEN BRANCHING ENZYME DEFICIENCY, FATAL PERINATAL NEUROMUSCULAR FORM


Glycogen storage disease VII is an autosomal recessive metabolic disorder characterized clinically by exercise intolerance, muscle cramping, exertional myopathy, and compensated hemolysis. Myoglobinuria may also occur. The deficiency of the muscle isoform of PFK results in a total and partial loss of muscle and red cell PFK activity, respectively. Raben and Sherman (1995) noted that not all patients with GSD VII seek medical care because in some cases it is a relatively mild disorder.

GLYCOGEN STORAGE DISEASE DUE TO GLYCOGEN BRANCHING ENZYME DEFICIENCY, FATAL PERINATAL NEUROMUSCULAR FORM Is also known as gsd due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form|glycogenosis type iv, fatal perinatal neuromuscular form|tarui disease|glycogenosis type 4, fatal perinatal neuromuscular form|gsd vii|gbe deficiency, fatal perinatal neur

Related symptoms:

  • Seizures
  • Muscle weakness
  • Pain
  • Anemia
  • Flexion contracture


SOURCES: OMIM ORPHANET MENDELIAN

More info about GLYCOGEN STORAGE DISEASE DUE TO GLYCOGEN BRANCHING ENZYME DEFICIENCY, FATAL PERINATAL NEUROMUSCULAR FORM

Top 5 symptoms//phenotypes associated to Arthritis and Nausea and vomiting

Symptoms // Phenotype % cases
Vomiting Common - Between 50% and 80% cases
Fever Common - Between 50% and 80% cases
Pain Uncommon - Between 30% and 50% cases
Myalgia Uncommon - Between 30% and 50% cases
Skin rash Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Seizures Arthralgia Fatigue Headache Short stature Lymphopenia Nausea Abdominal pain Anemia Diarrhea Erythema Sensorineural hearing impairment

Rare Symptoms - Less than 30% cases


Pneumonia Leukocytosis Intellectual disability Flexion contracture Asthenia Nail dystrophy Muscle weakness Pancytopenia Rheumatoid arthritis Chest pain Bilateral sensorineural hearing impairment Splenomegaly Hypertension Hearing impairment Decreased antibody level in blood Urticaria Failure to thrive Recurrent infections Immunodeficiency Respiratory failure Increased intracranial pressure Decreased methylcobalamin Kyphoscoliosis Thiamine-responsive megaloblastic anemia Hypothyroidism Severe short stature Generalized hypotonia Alopecia Kyphosis Edema Short neck Brachydactyly Feeding difficulties Scoliosis Respiratory distress Rickets Abnormality of the dentition Craniosynostosis Waddling gait Proptosis Constipation Pulmonary insufficiency Hypercalcemia Premature loss of primary teeth Chronic pain Chondrocalcinosis Papilledema Brachycephaly Premature loss of teeth Osteomalacia Bone pain Thoracic kyphosis Platyspondyly Reticulocytosis Hemolytic anemia Muscle cramps Cerebral visual impairment Exercise intolerance Easy fatigability Cholelithiasis Polycythemia Myoglobinuria Corneal opacity Gout Nonspherocytic hemolytic anemia Dark urine Increased total bilirubin Gastric ulcer Exercise-induced muscle cramps Exercise-induced myoglobinuria Increased muscle glycogen content Limb muscle weakness Jaundice Malabsorption Folate deficiency Genu valgum Postural instability Bowing of the long bones Chronic diarrhea Abnormal intestine morphology Cachexia Malnutrition Scleroderma Thoracolumbar scoliosis Elevated serum creatine phosphokinase Protein-losing enteropathy Mucopolysacchariduria Stiff neck Peripheral edema Intestinal polyp Cardiomyopathy Blindness Myopathy Septic arthritis Diffuse alveolar hemorrhage Hemolytic-uremic syndrome Keratoconjunctivitis Hoarse voice Oral-pharyngeal dysphagia Adrenal insufficiency Keratoconjunctivitis sicca Xerostomia Achalasia Nail dysplasia Asthma Epidermal acanthosis Psoriasiform dermatitis Osteomyelitis Pustule Parakeratosis Furrowed tongue Cholangitis Aspiration Cough Neutrophilia Abnormal lung morphology Hyperhidrosis Pruritus Dehydration Conjunctivitis Polydipsia Dysesthesia Hepatosplenomegaly Bronchiectasis Gastroesophageal reflux Vasculitis Inflammation of the large intestine Chronic lung disease Gastritis Bloody diarrhea Dysphagia Weight loss Chills Periostitis Anisocytosis Metabolic acidosis Secretory diarrhea Intellectual disability, mild Acidosis Pallor Autoimmunity Retinopathy Recurrent urinary tract infections Enterocolitis Leukopenia Combined immunodeficiency Macrocytic anemia Thrombocytosis Severe combined immunodeficiency Antinuclear antibody positivity Megaloblastic anemia Disseminated intravascular coagulation Increased serum ferritin Palmoplantar pustulosis Lower limb pain Geographic tongue Oligoarthritis Lymphadenopathy Episodic fever Recurrent aphthous stomatitis Elevated C-reactive protein level Lymphocytosis Neuritis Colitis Limb pain Malar rash Optic neuritis Tachycardia Decreased liver function Abnormality of the coagulation cascade Loss of consciousness Reduced erythrocyte 2,3-diphosphoglycerate concentration



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