Arthritis, and Pancreatitis

Diseases related with Arthritis and Pancreatitis

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


Top matches:

Low match NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1; NPHPL1


Nephronophthisis is an autosomal recessive cystic kidney disease characterized by onset of end-stage renal failure in the first 3 decades of life. The disorder is often associated with extrarenal manifestations, including liver fibrosis, retinal degeneration, and central nervous system abnormalities (summary by O'Toole et al., 2010).For a general phenotypic description and a discussion of genetic heterogeneity of nephronophthisis, see NPHP1 (OMIM ).

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1; NPHPL1

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

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Other less relevant matches:

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 FAMILIAL MEDITERRANEAN FEVER


Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent short episodes of fever and serositis resulting in pain in the abdomen, chest, joints and muscles.

FAMILIAL MEDITERRANEAN FEVER Is also known as benign paroxysmal peritonitis|familial paroxysmal polyserositis|benign recurrent polyserositis|polyserositis, familial paroxysmal|fmf|periodic disease|familial mediterranean fever, autosomal recessive|polyserositis, recurrent

Related symptoms:

  • Seizures
  • Pain
  • Anemia
  • Hepatomegaly
  • Fever


SOURCES: OMIM ORPHANET MENDELIAN

More info about FAMILIAL MEDITERRANEAN FEVER

Low match GLYCOGEN STORAGE DISEASE IA; GSD1A


Glycogen storage disease type I, also known as von Gierke disease, typically manifests during the first year of life with severe hypoglycemia and hepatomegaly caused by the accumulation of glycogen. Affected individuals exhibit growth retardation, delayed puberty, lactic acidemia, hyperlipidemia, hyperuricemia, and in adults a high incidence of hepatic adenomas (summary by Lei et al., 1993).

GLYCOGEN STORAGE DISEASE IA; GSD1A Is also known as gsd1|hepatorenal form of glycogen storage disease|hepatorenal glycogenosis|glucose-6-phosphatase deficiency|gsd ia|von gierke disease|glycogen storage disease i

Related symptoms:

  • Seizures
  • Short stature
  • Growth delay
  • Neoplasm
  • Muscular hypotonia


SOURCES: ORPHANET OMIM MENDELIAN

More info about GLYCOGEN STORAGE DISEASE IA; GSD1A

Low match GRANULOMATOSIS WITH POLYANGIITIS


Granulomatosis with polyangiitis is a small-vessel necrotizing vasculitis characterised by the association of inflammation of the vessel wall and peri- and extravascular granulomatosis.

GRANULOMATOSIS WITH POLYANGIITIS Is also known as wegener granulomatosis, formerly|gpa|wg, formerly

Related symptoms:

  • Seizures
  • Hearing impairment
  • Sensorineural hearing impairment
  • Pain
  • Visual impairment


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about GRANULOMATOSIS WITH POLYANGIITIS

Low 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

Low match HEMOCHROMATOSIS TYPE 2


Hemochromatosis type 2 (juvenile) is the early-onset and most severe form of rare hereditary hemochromatosis (HH; see this term), a group of diseases characterized by excessive tissue iron deposition of genetic origin.

HEMOCHROMATOSIS TYPE 2 Is also known as juvenile hemochromatosis

Related symptoms:

  • Muscle weakness
  • Pain
  • Hypertension
  • Hepatomegaly
  • Cardiomyopathy


SOURCES: OMIM ORPHANET MENDELIAN

More info about HEMOCHROMATOSIS TYPE 2

Low match RENAL CYSTS AND DIABETES SYNDROME


Renal cysts and diabetes syndrome (RCAD) is a rare form of maturity-onset diabetes of the young (MODY; see this term) characterized clinically by heterogeneous cystic renal disease and early-onset familial non-autoimmune diabetes. Pancreatic atrophy, liver dysfunction and genital tract anomalies are also features of the syndrome.

RENAL CYSTS AND DIABETES SYNDROME Is also known as renal dysfunction-early-onset diabetes syndrome|mody5|fjhn, atypical|cakut with diabetes|maturity-onset diabetes of the young, type 5|renal cysts-maturity-onset diabetes of the young syndrome|congenital anomalies of the kidney and urinary tract with diabe

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about RENAL CYSTS AND DIABETES SYNDROME

Top 5 symptoms//phenotypes associated to Arthritis and Pancreatitis

Symptoms // Phenotype % cases
Seizures Common - Between 50% and 80% cases
Renal insufficiency Common - Between 50% and 80% cases
Proteinuria Common - Between 50% and 80% cases
Hypertension Common - Between 50% and 80% cases
Gout Common - Between 50% and 80% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Hepatomegaly Pain Delayed puberty Elevated hepatic transaminase Nephropathy Abdominal pain Nephrolithiasis Chronic kidney disease Hyperuricemia Acidosis Osteoporosis Short stature Inflammation of the large intestine Nausea and vomiting Fever Vasculitis Meningitis Myocardial infarction Decreased glomerular filtration rate Diarrhea Splenomegaly Headache Arrhythmia Arthralgia Myalgia Chest pain Venous thrombosis Pericarditis Xanthelasma Hematuria Pleuritis Chronic pancreatitis Xanthomatosis Stage 5 chronic kidney disease Hypoglycemia Lactic acidosis Abnormality of the kidney Cardiomyopathy Hyperlipidemia Focal segmental glomerulosclerosis Hepatocellular carcinoma Hearing impairment Glomerulopathy

Rare Symptoms - Less than 30% cases


Papule Hemoptysis Recurrent respiratory infections Pleural effusion Cranial nerve paralysis Portal hypertension Abnormality of endocrine pancreas physiology Cough Myositis Pulmonary infiltrates Gangrene Paresthesia Nephrocalcinosis Purpura Epistaxis Rheumatoid arthritis Intestinal obstruction Subcutaneous nodule Increased serum ferritin Gastrointestinal hemorrhage Cerebral ischemia Elevated erythrocyte sedimentation rate Fatigue Intellectual disability Anemia Lymphadenopathy Growth delay Sensorineural hearing impairment Dilated cardiomyopathy Ataxia Renal cyst Visual loss Weight loss Increased inflammatory response Dyspnea Metabolic acidosis Diabetes mellitus Malabsorption Endocarditis Abnormality of the liver Hepatoblastoma Recurrent infections Lipemia retinalis Skin rash Erythema Stroke Retinopathy Neoplasm Doll-like facies Autoimmunity Orchitis Oral ulcer Enlarged kidney Protuberant abdomen Infertility Abnormal bleeding Anterior uveitis Optic neuritis Erythema nodosum Immunologic hypersensitivity Thrombophlebitis Alopecia areata Chorioretinitis Stomatitis Iridocyclitis Posterior uveitis Memory impairment Recurrent aphthous stomatitis Hemiparesis Dilatation Alopecia Glaucoma Reduced visual acuity Photophobia Developmental regression Irritability Joint stiffness Scarring Abnormal pyramidal sign Confusion Vertigo Migraine Abnormal blistering of the skin Mitral regurgitation Arterial thrombosis Anorexia Aortic regurgitation Increased intracranial pressure Encephalitis Acne Epiphora Blurred vision Keratoconjunctivitis sicca Pulmonary embolism Aseptic necrosis Uveitis Pustule Raynaud phenomenon Abnormal myocardium morphology Iritis Joint hyperflexibility Retrobulbar optic neuritis Bicornuate uterus Paraparesis Multicystic kidney dysplasia Spastic paraparesis Pyloric stenosis Polydipsia Unilateral renal agenesis Glucose intolerance Hypoplasia of the uterus Glycosuria Acute kidney injury Proportionate short stature Renal cell carcinoma Exocrine pancreatic insufficiency Elevated serum creatinine Maturity-onset diabetes of the young Renal dysplasia Absent vas deferens Atretic vas deferens Abnormality of exocrine pancreas physiology Aplasia/Hypoplasia of the pancreas Decreased numbers of nephrons Papillary cystadenoma of the epididymis Epididymal cyst Multiple glomerular cysts Biliary tract abnormality Renal cortical cysts Reduced sperm motility Renal Fanconi syndrome Uterus didelphys Pancreatic hypoplasia Ureteropelvic junction obstruction Horseshoe kidney Renal hypoplasia Superficial thrombophlebitis Hypogonadism Azoospermia Hypogonadotrophic hypogonadism Hyperpigmentation of the skin Amenorrhea Cirrhosis Lethargy Congestive heart failure Arthropathy Muscle weakness Hypopyon Decreased level of D-mannose in urine Epididymitis Genital ulcers Panuveitis Impotence Generalized hyperpigmentation Renal agenesis Cerebral cortical atrophy Hepatic steatosis Hirsutism Blindness Jaundice Mandibular prognathia Hypothyroidism Hypospadias Congenital hepatic fibrosis Abnormality of the dentition Global developmental delay Elevated transferrin saturation Abnormality of the anterior pituitary Abnormality of iron homeostasis Increased serum iron Behavioral abnormality Diplopia Gait disturbance Muscular hypotonia Anemia of inadequate production Peritonitis Decreased circulating aldosterone level Synovitis Stiff neck Congenital hypoplastic anemia Erysipelas Gastrointestinal infarctions Renal amyloidosis Azotemia Serositis Recurrent meningitis Cognitive impairment Acute hepatic failure Myopathy Osteopenia Carcinoma Hepatic failure Full cheeks Hepatitis Hypertriglyceridemia Atherosclerosis Hypercalciuria Elevated alkaline phosphatase Glomerulosclerosis Decreased muscle mass Oral leukoplakia Edema of the lower limbs Renal tubular acidosis Neutropenia Tremor Retinal degeneration Nephronophthisis Arachnoid cyst Tubular atrophy Kinetic tremor Pancreatic cysts Renal corticomedullary cysts Tubular basement membrane disintegration Pulmonary arterial hypertension Spider hemangioma Ketonemia Recurrent bacterial infections Antinuclear antibody positivity Constipation Hepatosplenomegaly Nausea Ascites Asthma Nephrotic syndrome Osteoarthritis Systemic lupus erythematosus Leukocytosis Hyperkalemia Amyloidosis Episodic fever Prolonged bleeding time Neoplasm of the liver Hyperreflexia Periorbital edema Petechiae Wheezing Tracheal stenosis Chronic obstructive pulmonary disease Angina pectoris Concave nasal ridge Abnormality of the nose Abnormality of the hypothalamus-pituitary axis Recurrent corneal erosions Nasal obstruction Inflammatory abnormality of the eye Elevated C-reactive protein level Rhinorrhea Pulmonary fibrosis Ocular pain Subglottic stenosis Granulomatosis Neuritis Ureteral stenosis Abnormal oral cavity morphology Episcleritis Arteritis Scleritis Recurrent intrapulmonary hemorrhage Prostatitis Cataract Restrictive ventilatory defect Diabetes insipidus Breathing dysregulation Peripheral neuropathy Fasting hypoglycemia Skeletal myopathy Enterocolitis Pyelonephritis Hypoglycemic seizures Microalbuminuria Intermittent diarrhea Chronic hepatitis Distal renal tubular acidosis Hepatocellular adenoma Hypocitraturia Visual impairment Respiratory insufficiency Stridor Respiratory distress Proptosis Hydronephrosis Paralysis Sensory neuropathy Otitis media Sinusitis Skin ulcer Hoarse voice Conjunctivitis Hemiplegia Glomerulonephritis Chronic otitis media Abnormality of alkaline phosphatase activity



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