Disease Comparison Results (show all mode) for Hemochromatosis and Mixed connective tissue disease (MCTD)/Undifferentiated

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Hemochromatosis

Found: 330 | Differences: 301

Hemochromatosis and Mixed connective tissue disease (MCTD)/Undifferentiated sharing 29 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Facial Malar flush/rash
Plethora/Red face/Ruddy look
Nailfold capillary/giant loops sign
Baldness/Alopecia
Facial rash
Hair loss
Non-scarring Alopecia/balding
Photosensitivity/Sunsensitive skin
Rash
Skin thickening over fingers
Tightness of skin/sensation
Anorexia Decreased appetite
Dry mouth/Mucous membranes
Gingival Tenderness Pain
Oral lesion/ulcer
Painful oral ulcers
Parotid swelling
Salivary Gland Enlargement
Sore Gums
Cold hands/fingers and toes
Diffuse Aches and Pains
Finger swelling
Fingers, 'sausage' shaped
Hand edema/swelling
Hand pain and swelling/unilateral
Hand Pains
Hand/Wrist Pain Unilateral
Hand/wrists induration/pain/edema
Muscle Pain
Muscle weakness
Myalgias
Proximal lower extremity weakness
Proximal muscle weakness
Proximal upper extremity weakness
Arthralgias Polyarthralgias
Arthritis Children
Arthritis with Muscle Weakness
Joint Pains
Joint pains Arthralgias in Elderly
Monoarticular Arthritis in Elderly
Monoarticular Arthritis/One joint acute
Morning gel stiffness
Multiple Joint Arthritis
Polyarticular Joint Pain
Skeletal problems/symptoms/signs
Stiffness of joints
Chronic Fatigue
Constitutional symptoms
Fatigue
Fatigue Tiredness Exhaustion
Fever
Fever Febrile Possible
Fever of unknown origin/chronic fever
Flu-Like Syndrome
High body temperature
Malaise
Weakness non-neuromuscular/systemic
Weight Loss
Dry eyes/poor tearing
Dryness Conjunctiva
Grainy/Gritty Eye Sensation
Clinical Presentation & Variations
Pulmonary Renal Syndromes
Muscle Weakness with Polyarthritis Presentation
presentation/Acute polyarthritis syndrome Days
Presentation/Single Joint Arthritis
Fever and High Sed Rate
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Established Disease Population
Patient/Mitral valve prolapse
Population Group
Woman
Sex & Age Groups
Population/Adult ('twenties')
Population/Adult Aged Only
Population/Adult/all
Population/Female
Population/Fifties adult
Population/Forties adult
Population/Middle-aged adult
Population/Post-menopausal female
Population/Thirties adult
Population/Woman patient
Laboratory Tests
Microbiology & Serology Findings
Serum specific antibodies increased
Anti-DNA Antibodies
Abnormal Lab Findings (Non Measured)
Acute inflammatory markers elevated (Lab)
Gamma globulin polyclonal very high
Abnormal Lab Findings - Decreased
Complement (total CH50) level (Lab)
Abnormal Lab Findings - Increased
Anti-cardiolipin (Lab)
Anti-DNA-Histone (DNP) antibodies (Lab)
Anti-Ku antibody (labs)
Antiphospholipid antibodies (Lab)
Anti-RNA antibody/Nrnp (Lab)
Anti-RNP (U1RNP) antibody (Lab)
Anti-Smooth muscle (actin) antibodies (Lab)
Anti-ssDNA (single stranded) antibody (Lab)
Antithyroglobulin antibodies (Lab)
Anti-DNA antibody (Double stranded/Native) (Lab)
Anti-RNA-RNP/ENA Sm (Smith) antibody (Lab)
Aldolase, serum (Lab)
ANA, homogenous/serum (Lab)
ANA, peripheral/serum (Lab)
ANA, speckled (Lab)
ANA/Antinuclear antibody/Fluorescent ANA (Lab)
Anti-DNA Antibody
Anti-ENA (Extractable Nuclear Antigen) Level
Anti-Nuclear Antibody (ANA)
Anti-SSA (Ro) Antibody
CPK/CK/Creatine kinase/Creatine phosphokinase (Lab)
C-reactive protein (Lab)
Gamma globulin (Lab)
IGG/Immunoglobulin G (Lab)
LE Prep/Lupus erythematosis cell prep (Lab)
Rheumatoid factor (Lab)
Sed Rate/ESR/Sedimentation rate (Lab)
Diagnostic Test Results
Other Tests & Procedures
PFT/Diffusion defect
Pathology
PATH/Proliferation plasma cells/lymphocytes
Electrodiagnosis
EMG/Abnormal findings
EMG/Inflammatory type
X-RAY
Xray/Chest abnormal
Xray/Chest/Lung fields/Abnormal
Xray/Pulmonary fibrosis/Chest
Ultrasound
Echo/Pulmonary artery hypertension
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Dermatomyositis
Associated Disease & Complications - Causes
Acrosclerosis
Alopecia areata
Alopecia totalis/universalis
Anemia
Arthritis
Carpal tunnel syndrome
Dermatomyositis
Esophageal motility disorder
Hypertrophic osteoarthropathy
Hypocomplementemia
Inflammatory myopathy
Lupus erythematosis, systemic
Membranous Nephropathy
Mikulicz's Syndrome
Mitral valve prolapse syndrome
Mixed connective tissue disease (MCTD)
Mononeuritis, multiplex
Multi-radicular Polyneuropathy syndrome
Pericarditis, acute
Photosensitivity dermatitis
Phototoxicity
Polyarthritis in Children
Polyarthritis syndrome/Multiple joints/weeks
Polymyositis
Polyserositis syndrome
Psychosis
Pulmonary fibrosis
Pulmonary hypertension
Raynaud's disease
Raynaud's syndrome
Sclerodactyly
Scleroderma esophagus
Scleroderma renal disease
Scleroderma, progressive systemic
Tendonitis
Xerophthalmia
Xerostomia
Monoarthritis Acute
PolyArthritis
Disease Mechanism & Classification
Class
CLASS/Connective tissue/Mesenchyme matrix disorder
CLASS/Tissue/cells/organelles/collagen (category)
Pathophysiology
Pathophysiology/Multisystem disease
Pathophysiology/Exertional O2 desaturation
Process
PROCESS/Allergy/collagen/autoimmune (category)
PROCESS/Systemic illness (ex)
Synonyms
Synonym
Synonym/Overlap Connective Dis Variant
Synonym/UCTD
Synonym/Undifferentiated Connective Tissue Disease
Treatment
Drug Therapy
RX/Corticosteroid (Cortisone)
RX/Immune-suppression
RX/Non-steroidal anti-inflammatory drugs
Clinical Manifestations
Signs & Symptoms
Breast Swelling Bilateral
Arrhythmia signs/irregular pulse
Cardiac Symptoms/Signs
Cardiomegaly/Heart dilatation
Chronic hypotension
Bronze Skin Color
Brown skin discoloration
Extensor surfaces/skin manifestations
Increased pigmentation/tanning/hyperpigmented
Koilonychia/Spoon nails
Loss of body hair/thinning
Slate gray pigmentations
Spider nevi/angiomata/Abdominal sign
Subcutaneous nodules
Yellow skin discoloration
Loss of libido,male
Sexual dysfunction
Small testes
Small/soft testes
Abdominal Pain
Hepatosplenomegaly
Jaundice/Yellow skin and eyes
Liver firm/edge indurated
Liver palms/erythema
Palpable Liver/Hepatomegaly
Yellow eyeballs/Scleral icterus
Cramping in Extremities
Hand Pains
Muscle cramps/spasms
Muscle Pain
Myalgias
Pain in Extremities/Melalgias
Palmar Erythema/Redness
Tender or painful muscles/Myalgias
Weak/Weak as a kitten (symptom)
Apathy/Indifference
Fatigability
Hyperesthesia
Lethargy/torpor
Neurological symptoms/signs
Spasms in Both Legs
Amenorrhea
Amenorrhea, secondary
Loss of libido,women
Dyspnea on exertion
Arthralgias Polyarthralgias
Arthritis Children
Arthritis of major joint
Arthritis with Abdominal Pain
Asymmetric Oligoarthropathy
Joint exam/signs
Joint Pains
Joint pains Arthralgias in Children
Joint pains Arthralgias in Elderly
Large joint involvement/manifestation
Metacarpophalangeal arthritis/signs
Monoarticular Arthritis/One joint acute
Multiple Joint Arthritis
Oligoarthritis syndrome/signs
Polyarticular Joint Pain
Shoulder arthritis signs/symptoms
Symmetrical Osteoarthritis Bilateral metacarpal joints
Wrist arthritis/signs
Splenomegaly
Chronic Fatigue
Enervated/extreme acute fatigue
Fatigue
Fatigue Tiredness Exhaustion
Fatigue Tiredness in Elderly
Listlessness/lassitude
Weakness
Weakness non-neuromuscular/systemic
Weight Loss
Dry eyes/poor tearing
Dry eyes/Poor tearing in Children
Dry eyes/Poor tearing in Elderly
Dryness Conjunctiva
Grainy/Gritty Eye Sensation
Calcification/pinna cartilage/sign
Typical Clinical Presentation
Arthritis with Subcutaneous/Skin Nodules
Presentation/Fatigue, Arthritis, Loss Libido
Clinical Presentation & Variations
Presentation/Congestive heart failure Child
Presentation/Diabetic Decreased need for Insulin
Presentation/Liver Pancreas Heart Endocrine Involvement
Presentation/Pancreatitis Kids Recurrent
Presentation/Aggressive Osteoarthritis
Presentation/Osteoarthritis Knuckle Joints Agressive (Index Long)
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Ethnic or Racial Factors
Population Caucasian/White
Established Disease Population
Patient/Hemochromatosis
Population Group
Child
Man
Population/Pediatrics population
Family History
Family history/Diabetes mellitus
Family history/Endocrine disorder
Family history/Liver disease
Family history/Arthritis
Sex & Age Groups
Population/Adult Aged Only
Population/Adult/all
Population/Child
Population/Children/all
Population/Male
Population/Man patient
Laboratory Tests
Abnormal Lab Findings (Non Measured)
Chromosomal abnormality (Lab)
DNATest specific/genetics laboratory/abnormality (Lab)
Ferritin extremely high (Lab)
Gene mutation C282Y Test Positive
Gene mutation H63D Test Positive
Hepatic Enzymes Abnormal (Lab)
HFE Gene mutations
HFE mutation (C282Y or H63D) positive (Lab)
Liver Functions Abnormal (Lab)
Transaminase elevation (Lab)
HLA A3 (Lab)
HLA B27 (Lab)
Abnormal Lab Findings - Decreased
ACTH/Corticotrpin/Adrenocortical Hypertrophic hormone (Lab)
Androgens (Lab)
Ascorbic acid/Vitamin C (Lab)
Cortisol (Lab)
Growth hormone/STH, plasma (Lab)
LH/Leutinizing Hormone (Lab)
Testosterone Total (Lab)
TIBC/Total Iron Binding capacity (Lab)
Transferrin (Lab)
Transferrin receptor index
Uric acid, serum (Lab)
URINE 17-Ketosteroids
Abnormal Lab Findings - Increased
Alkaline phosphatase, liver isoenzyme/serum (Lab)
Alkaline phosphatase, serum (Lab)
ALT (SGPT) (Alanine transferase) (Lab)
Ammonia blood (Lab)
Aspartamine aminotransferase (SGOT, AST) (Lab)
AST (SGOT) (aspartamine transferase) (Lab)
Bilirubin, serum (Lab)
Copper, serum (Lab)
Ferritin, serum (Lab)
FSH/Follicle Stmulating Hormone/ICSH (Lab)
Gammaglutamyl transferase/GGT (Lab)
Glucose, blood (Lab)
Indirect bilirubin (Lab)
Iron, serum (Lab)
LAP/Leucine Amino Peptidase (Lab)
Nucleotidase/5 (Lab)
Potassium, serum (Lab)
Saturated iron binding capacity (Lab)
Transferrin (Lab)
Transferrin saturation (Lab)
URINE Growth hormone
URINE Hemosiderin
Diagnostic Test Results
Other Tests & Procedures
Heart cath/Left ventricle end-diastolic pressure inc
Gastroscopy/Esophageal varices
Pathology
PATH/Myocardial pathology/Fibrosis
Bone Marrow/Iron stores/increased
Bone Marrow/RES iron increased
BX/Hepatic Iron Index Abnormal
BX/Liver biopsy/Abnormal
BX/Liver biopsy/Diagnostic
BX/Liver biopsy/Increased liver iron stores
PATH/Pancreatic biopsy/Abnormal
BX/Synovial abnormal
Isotope Scan
MUGA Scan/Diastolic first derivative slow
EKG (ECG)
EKG/Prolonged PR Interval (ECG)
EKG/AV Nodal Block/Complete
EKG/Bifascicular hemiblock (ECG)
EKG/Conduction defect findings (ECG)
EKG/Changes/abnormalities (ECG)
CT Scan
MRI/Heart scan myocardial texture change
CT/Liver High Density/ABD
MRI/Ferriscan liver abnormal
MRI/Liver abnormal density
CT/Dexa-Scan Bone density Abnormal
X-RAY
Xray/Chest abnormal
Xray/Congestive heart failure signs/Chest
Xray/Large heart shadow/Chest
Xray/Abdominal calcifications/ABD
Xray/Abdominal film abnormalities/ABD/KUB
Xray/Liver calcification/ABD
Xray/Chest/Lung fields/Abnormal
Xray/Calcification of intervertebral disk
Xray/Chondrocalcinosis/knees
Xray/Joint abnormal
Xray/Joint cartilage calcification
Xray/Joint/cartilage erosion signs
Xray/Metacarpal Phalangeal Joint Erosion
Xray/Metacarpal-phalangeal hook-like osteophytes
Xray/Ossification/calcification lumbar disks/LS spine
Xray/Osteophytes
Xray/Subchondral cysts/Joint
Xray/Calcification ear cartilage/Skull
X-RAY With contrast
UGI/Esophageal varices
Ultrasound
Echo/Poor filling ventricles
Echo/Stiff ventricular wall motion
Ultrasound/Abdomen/Liver small
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Addison's disease
Autoimmune hepatitis
Hemosiderosis
Hepatic vein thrombosis (Budd-Chiari)
Non-alcoholic fatty liver disease
Osteoarthritis, degenerative
Polyglandular autoimmune syndrome
Portal hypertension
Chronic Hepatitis
Associated Disease & Complications - Causes
Addison's disease
Adrenocortical insufficiency
Anorchia/Hypoplasia testes
Arthritis
Arthropathy, destructive/erosive
Ascites
AV node lesion/infiltrate
Bilirubinemia
Bradyarrhythmias
Capnocytophaga Canimorsus (CDC group DF2)
Carcinoma, hepatocellular
Cardiac arrhythmias
Cardiac conduction defects
Cardiomyopathy
Cardiomyopathy, dilated
Cardiomyopathy, hemochromatosis
Cardiomyopathy, restrictive
Cardiomyopathy, secondary
CHF with Preserved Ejection Fraction
Cholelithiasis
Chondrocalcinosis, articular
Chronic hepatitis/Active
Cirrhosis
Cirrhosis/complication/secondary
Congestive heart failure
Diabetes mellitus
Endocrine dysfunction
Esophageal varices
Glucocorticoid Deficiency
Gynecomastia
Heart block, complete
Hemochromatosis
Hepatic encephalopathy
Hip arthritis
Hyperammonemia
Hyperglycemia
Hyperpigmentation
Hypogonadism, male
Hypoparathyroidism, primary
Hypoparathyroidism/secondary
Hypothyroidism (myxedema)
Hypouricemia
Impotence/Erectile dysfunction disorder
Infertility/sterility, female
Infiltrative cardiomyopathy
Knee arthritis
Left Ventricular Failure
Listeria meningitis
Male osteoporosis syndrome
Metacarpal DJD/Second and Third Severe
Myocarditis, acute
Osteoarthritis in Young Adults
Osteoarthritis, degenerative
Osteoporosis/osteopenia
Pancreatitis, chronic/recurrent
Panhypopituitarism
Pathologic fractures
Peritoneal Effusion
Pituitary hypothyroidism
Pituitary ischemic necrosis
PolyArthritis in Elderly
Polyarthritis syndrome/Multiple joints/weeks
Portal hypertension
Pseudogout (CPPD) arthritis
Secondary female hypogonadism
Shoulder osteoarthritis
Supraventricular tachycardia
Synovitis/arthritis
Testicular atrophy
Vibriosis/non-cholera
Yersinia enterocolitis syndrome
Heart Failure in a Child
Iron Overload
Chronic Hepatitis
Diabetes mellitus/non-insulin dep/type II
Metabolic Bone Disease
Monoarthritis Acute
PolyArthritis
Disease Mechanism & Classification
Class
CLASS/Chronic liver disease (ex)
CLASS/Second/third metacarpal phalangeal joint/manifestation
CLASS/Systemic/no comment (category)
Pathophysiology
Pathophysiology/Gene locus 6p21.3
Pathophysiology/Gene locus Chromosome 6
Pathophysiology/Gene locus Chromosome 6p
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Homozygous for Disease
Pathophysiology/Multisystem disease
Pathophysiology/Single gene locus indentified
Pathophysiology/Cardiac Diastolic Compliance Decreased
Pathophysiology/Delayed Diastolic Relaxation
Pathophysiology/Diastolic left ventricular dysfunct/failure
Pathophysiology/Diastolic-type heart failure/poor filling
Pathophysiology/High end-diastolic pressures (ex)
Pathophysiology/Inadequate ventricular diastolic filling
Pathophysiology/Myocardial infiltrate/Infiltrative (ex)
Pathophysiology/Adrenal destruction/atrophy/infiltrate
Pathophysiology/Hypogonadotrophic hypogonadism
Pathophysiology/Primary Testicular Failure
Pathophysiology/HFE Gene mutation H63D
Pathophysiology/HFE gene mutation/C282Y mutation
Pathophysiology/Bleeding from Portal Veins
Pathophysiology/Osteoporosis Secondary
Process
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Enzyme defect/Metabolic disorder (ex)
PROCESS/Ethnic predilection (ex)
PROCESS/Hereditofamilial (category)
PROCESS/Metabolic/storage disorder (category)
PROCESS/Storage disorder (ex)
Synonyms
Synonym
Gene Mutation 565C Test Positive
MRI/Hyperdense Liver Black Appearing/ABD
Synonym/Bronze diabetes
Treatment
Drug Therapy - Contraindication
RX/Ascorbic acid/Vitamin C
RX/Iron/Ferrous Sulfate (Feosol)
Drug Therapy - Indication
RX/Chelating agent
RX/Deferasirox (Exjade)
RX/Deferoxamine (Desferal)
Surgical Procedures or Treatments
SX/Biopsy
SX/Liver biopsy
Other Treatments
TX/Phlebotomy.
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