Arthritis, and Proteinuria

Diseases related with Arthritis and Proteinuria

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


Top matches:

Low match PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE


PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE Is also known as papas|familial recurrent arthritis|papa syndrome|fra

Related symptoms:

  • Diabetes mellitus
  • Arthritis
  • Proteinuria
  • Type I diabetes mellitus
  • Acne


SOURCES: OMIM MENDELIAN

More info about PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE

Low match FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT


FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT Is also known as fmf, autosomal dominant

Related symptoms:

  • Pain
  • Fever
  • Renal insufficiency
  • Abdominal pain
  • Arthralgia


SOURCES: MESH OMIM MENDELIAN

More info about FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT

Low match PYOGENIC ARTHRITIS-PYODERMA GANGRENOSUM-ACNE SYNDROME


Pyogenic arthritis-pyoderma gangrenosum-acne syndrome is a rare pleiotropic autoinflammatory disorder of childhood, primarily affecting the joints and skin.

PYOGENIC ARTHRITIS-PYODERMA GANGRENOSUM-ACNE SYNDROME Is also known as familial recurrent arthritis|papa syndrome|fra

Related symptoms:

  • Fever
  • Fatigue
  • Arthralgia
  • Arthritis
  • Proteinuria


SOURCES: ORPHANET MENDELIAN

More info about PYOGENIC ARTHRITIS-PYODERMA GANGRENOSUM-ACNE SYNDROME

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Other less relevant matches:

Low match HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4


Related symptoms:

  • Short stature
  • Growth delay
  • Cleft palate
  • Cognitive impairment
  • Anemia


SOURCES: OMIM MENDELIAN

More info about HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4

Low match IMMUNODEFICIENCY WITH FACTOR I ANOMALY


Immunodeficiency with factor I anomaly is a rare, genetic, primary immunodeficiency disease characterized by increased susceptibility to recurrent, usually severe, infections (particularly by Neisseria meningitidis, Haemophilus influenzae and Streptococcus pneumonia), typically manifesting as otitis, sinusitis, bronchitis, pneumonia, and/or meningitis. Autoimmune disease (e.g. systemic lupus erythematosus, glomerulonephritis) and atypical hemolytic uremic syndrome may be associated. Laboratory serum analysis reveals, in addition to diminished or undetectable complement factor I, variably decreased complement C3, complement factor B and complement factor H.

IMMUNODEFICIENCY WITH FACTOR I ANOMALY Is also known as complement component 3 inactivator deficiency|c3 inactivator deficiency

Related symptoms:

  • Fever
  • Renal insufficiency
  • Recurrent infections
  • Pneumonia
  • Recurrent respiratory infections


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about IMMUNODEFICIENCY WITH FACTOR I ANOMALY

Low match MEDULLARY SPONGE KIDNEY


Medullary cystic kidney disease (MCKD) is an autosomal dominant form of tubulointerstitial nephropathy characterized by formation of renal cysts at the corticomedullary junction. It is characterized by adult onset of impaired renal function and salt wasting resulting in end-stage renal failure by the sixth decade (Wolf et al., 2004).Although early reports suggested that medullary cystic kidney disease and familial juvenile nephronophthisis (NPHP1 ) represented the same disease entity because of the overlapping phenotype (Chamberlin et al., 1977), they are now considered to be distinct disorders. MCKD has adult onset and shows autosomal dominant inheritance, whereas NPHP1 has juvenile onset and shows autosomal recessive inheritance (Christodoulou et al., 1998). NPHP1 is caused by mutation in the nephrocystin gene (NPHP1 ) on chromosome 2q13. Genetic Heterogeneity of Medullary Cystic Kidney DiseaseSee also MCKD2 (OMIM ), which is caused by mutation in the UMOD gene (OMIM ) on chromosome 16p.

MEDULLARY SPONGE KIDNEY Is also known as cacchi-ricci disease|msk|medullary cystic kidney disease, autosomal dominant|admckd1|polycystic kidneys, medullary type|mckd|precalicial canalicular ectasia

Related symptoms:

  • Pain
  • Anemia
  • Hypertension
  • Renal insufficiency
  • Cerebral cortical atrophy


SOURCES: ORPHANET OMIM MENDELIAN

More info about MEDULLARY SPONGE KIDNEY

Low match NAIL-PATELLA SYNDROME


Nail-patella syndrome (NPS) is a rare hereditary patellar dysostosis characterized by nail hypoplasia or aplasia, aplastic or hypoplastic patellae, elbow dysplasia, and the presence of iliac horns as well as renal and ocular anomalies.

NAIL-PATELLA SYNDROME Is also known as turner-kieser syndrome|onychoosteodysplasia

Related symptoms:

  • Hearing impairment
  • Cataract
  • Hypertension
  • Renal insufficiency
  • Glaucoma


SOURCES: ORPHANET MENDELIAN

More info about NAIL-PATELLA SYNDROME

Low match GLYCOGEN STORAGE DISEASE IC; GSD1C


GLYCOGEN STORAGE DISEASE IC; GSD1C Is also known as gsd ic

Related symptoms:

  • Hypertension
  • Hepatomegaly
  • Renal insufficiency
  • Hypoglycemia
  • Proteinuria


SOURCES: ORPHANET OMIM MENDELIAN

More info about GLYCOGEN STORAGE DISEASE IC; GSD1C

Low match GLYCOGEN STORAGE DISEASE DUE TO GLUCOSE-6-PHOSPHATASE DEFICIENCY TYPE IB


Glycogenosis due to glucose-6-phosphatase deficiency (G6P) type b, or glycogen storage disease (GSD) type 1b, is a type of glycogenosis due to G6P deficiency (see this term).

GLYCOGEN STORAGE DISEASE DUE TO GLUCOSE-6-PHOSPHATASE DEFICIENCY TYPE IB Is also known as glycogenosis due to glucose-6-phosphatase transport defect type ib|gsd type ib|glycogenosis due to glucose-6-phosphatase deficiency type 1b|glycogen storage disease type ib|gsd due to g6p deficiency type ib|glycogen storage disease due to g6p deficiency t

Related symptoms:

  • Seizures
  • Short stature
  • Growth delay
  • Hypertension
  • Hepatomegaly


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about GLYCOGEN STORAGE DISEASE DUE TO GLUCOSE-6-PHOSPHATASE DEFICIENCY TYPE IB

Low match HYPOCOMPLEMENTEMIC URTICARIAL VASCULITIS


Hypocomplementemic urticarial vasculitis (HUV) is an immune complex-mediated small vessel vasculitis characterized by urticaria and hypocomplementemia (low C1q with or without low C3 and C4), and usually associated with circulating anti-C1q autoantibodies. Arthritis, pulmonary disease, ocular inflammation, and glomerulonephritis are common systemic manifestations.

HYPOCOMPLEMENTEMIC URTICARIAL VASCULITIS Is also known as mac duffie syndrome|mac duffie hypocomplementemic urticarial vasculitis|anti-c1q vasculitis|mcduffie hypocomplementemic urticarial vasculitis|mcduffie syndrome

Related symptoms:

  • Seizures
  • Ataxia
  • Sensorineural hearing impairment
  • Pain
  • Peripheral neuropathy


SOURCES: ORPHANET MENDELIAN

More info about HYPOCOMPLEMENTEMIC URTICARIAL VASCULITIS

Top 5 symptoms//phenotypes associated to Arthritis and Proteinuria

Symptoms // Phenotype % cases
Hematuria Common - Between 50% and 80% cases
Renal insufficiency Common - Between 50% and 80% cases
Hypertension Uncommon - Between 30% and 50% cases
Gout Uncommon - Between 30% and 50% cases
Recurrent infections Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Nephropathy Decreased glomerular filtration rate Chronic kidney disease Focal segmental glomerulosclerosis Hyperuricemia Nephritis Arthralgia Pain Recurrent bacterial infections Vasculitis Hepatomegaly Fever

Rare Symptoms - Less than 30% cases


Lactic acidosis Xanthomatosis Delayed puberty Xanthelasma Hyperlipidemia Neutropenia Meningitis Hepatocellular carcinoma Elevated serum creatinine Nephrolithiasis Abnormality of the kidney Hypoglycemia Seizures Renal cyst Anemia Stage 5 chronic kidney disease Lymphadenopathy Abdominal pain Growth delay Glomerulopathy Short stature Type I diabetes mellitus Joint dislocation Acne Osteoarthritis Hepatoblastoma Chronic pancreatitis Aplastic/hypoplastic toenail Spider hemangioma Pulmonary arterial hypertension Joint hyperflexibility Ketonemia Osteoporosis Acidosis Nephrotic syndrome Cubitus valgus Metabolic acidosis Abnormality of the lower limb Elevated hepatic transaminase Thickening of the lateral border of the scapula Aplasia/Hypoplasia of the patella Concave nail Ridged nail Abnormality of the upper limb Abnormal toenail morphology Abnormality of the fingernails Abnormality of the elbow Patellar dislocation Exostoses Joint swelling Hypoplastic toenails Iliac horns Diabetes mellitus Diarrhea Abnormal bleeding Abnormal heart valve morphology Cerebral palsy Reduced tendon reflexes Urticaria Pleural effusion Hemiplegia/hemiparesis Emphysema Restrictive ventilatory defect Pericardial effusion Hemoptysis Conjunctivitis Irregular hyperpigmentation Uveitis Inflammatory abnormality of the eye Angioedema Complement deficiency Immunologic hypersensitivity Episcleritis Obstructive lung disease Cranial nerve paralysis Lymphoma Pancreatitis Peripheral neuropathy Inflammation of the large intestine Protuberant abdomen Enlarged kidney Oral ulcer Lipemia retinalis Doll-like facies Ataxia Sensorineural hearing impairment Skeletal dysplasia Ascites Splenomegaly Dyspnea Myalgia Autoimmunity Skin rash Cough Pruritus Nausea and vomiting Sensory neuropathy Joint stiffness Thin bony cortex Glaucoma Pneumonia Intrauterine growth retardation Dilatation Polydactyly Postnatal growth retardation Bifid uvula Preaxial polydactyly Velopharyngeal insufficiency Recurrent respiratory infections Cleft palate Respiratory tract infection Sepsis Otitis media Recurrent otitis media Recurrent urinary tract infections Sinusitis Purpura Recurrent skin infections Cognitive impairment Increased inflammatory response Glomerulonephritis Pleuritis Juvenile rheumatoid arthritis Pyoderma Pyoderma gangrenosum Sterile arthritis Chest pain Amyloidosis Episodic fever Peritonitis Erysipelas Crohn's disease Renal amyloidosis Polyarticular arthritis Fatigue Limitation of joint mobility Skin ulcer Increased antibody level in blood Pustule Myositis Systemic lupus erythematosus Recurrent sinusitis Cataract Renal cortical cysts Tubulointerstitial nephritis Fair hair Renal salt wasting Tubular atrophy Hemihypertrophy Tubulointerstitial fibrosis Distal renal tubular acidosis Tubulointerstitial abnormality Flank pain Polyuria Renal corticomedullary cysts Multiple small medullary renal cysts Tubular basement membrane disintegration Global glomerulosclerosis Pyuria Impaired renal uric acid clearance Renal cortical atrophy Hearing impairment Nephronophthisis Polydipsia Pyelonephritis Decreased serum complement factor B Hemolytic-uremic syndrome Mesangial hypercellularity Septic arthritis Decreased serum complement C3 Recurrent streptococcus pneumoniae infections Tonsillitis Recurrent meningococcal disease Recurrent meningitis Decreased serum complement factor H Glomerulosclerosis Decreased serum complement factor I Glomerular deposits Recurrent Haemophilus influenzae infections Cerebral cortical atrophy Hypotension Renal hypoplasia Hypercalciuria Polycystic kidney dysplasia Small vessel vasculitis



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