Categories

Conditions Observed

Allergies

Allergic Asthma
Allergic Rhinitis
Allergies in General
Allergy to Nuts
Allergy to Pets
Allergy to Shrimp
Allergy to mites
Allergy to pollen
Asthma
Atopic Dermatitis
Cockroach allergy
Cold-induced hives
Contact dermatitis
Eczema
Egg White Allergy
Grass allergy
Histamine Intolerance
IgE
Mast Cell Activation Syndrome (MCAS)
Milk Allergy
Peach Allergy
Peanut Allergy

Cancer

Thyroid Neoplasm
 

Cardiovascular

Prothrombin (G20210A Mutation)

Cardiovascular and Cerebrovascular

Phospholipase Cg2 Defect
 

Cells

Autophagy

Diabetes

Early Type 2 Diabetes
MODY Type 1 Diabetes
MODY Type 2 Diabetes
MODY Type 3 Diabetes
MODY Type 4 Diabetes
MODY Type 5 Diabetes
MODY Type 6 Diabetes
MODY Type Diabetes
Type 1 Diabetes
Type 2 diabetes

Digestive system

Hirschsprung’s Disease (HD)
Permeable Intestine Syndrome
Primary Biliary Cirrhosis (CBP)
Ulcerative Colitis

Endocrine system

Autoimmune Thyroid Disease
Hashimoto’s Thyroiditis
Hashimoto’s Thyroiditis (in children)
Hyperparathyroidism
Hyperthyroidism
Hypothyroidism
Hypothyroidism (Goiter)
T3
Thyroid Orbitopathy (OT)
Thyroid dyshormonogenesis
Thyrotoxicosis

Genetic diseases

Familial Amyloidotic Polyneuropathy (FAP)
Family Mediterranean Fever
Hereditary angioedema
Hyperimmunoglobulin E (Hyper IgE) Syndrome
Rasopathies
Selective IgA Deficiency

Hematologic system

Activated partial thromboplastin time (aPTT)
Alpha-Defensins Levels
Hemolytic Anemia
High ferritin (in men)
Post-Transfusion Purpura (PPT)
Tendency to have Increased Eosinophils in Contact with Allergens
Thrombophilia (Factor V – Protein C)

Hormone

Change of Timo
Reduction of Thyroid Hormonal Metabolism
TSH
Thyroid Function
Thyroid Hormone Metabolism (T3: T4 Reduced Ratio)

Immune system

Acquired Immune Response
Ankylosing spondylitis
Anti-Beta-2-Glycoprotein Antibody
Anti-DNA Antibody
Anticardiolipin Antib.
Antiphospholipid Antibody Syndrome
Antithrombin Deficiency
Autoimmune Lymphoproliferative Syndrome (ALPS)
B Lymphocyte Deficiency
C3 (immune) deficiency
Chronic Granulomatous Disease (CGD)
Combined immunodeficiency due to magnesium deficiency (XMEN)
Common Variable Immunodeficiency – type 1
Common Variable Immunodeficiency – type 2
Common Variable Immunodeficiency – type 8
Crohn’s disease
Defect in Thyroid Hormonogenesis
Dermatomyositis
Factor V Leiden Mutation
Familial hemophagocytic lymphohistiocytosis (HLH)
Graves’ Disease
Guillain-Barré Syndrome
HLA-DQ2.2
HLA-DQ2.5
HLA-DQ4
HLA-DQ7
HLA-DQ8
Herpes
Immunodeficiency with Hyper IgM – type 1
Increased Susceptibility to Contracting HIV-1
Lichen Planus
Lupus
Lupus anticoagulant
Lymphedema
MYD88 deficiency
Mannose Binding Protein Deficiency
Mutation of the SERPINE1 Gene (PAI-1)
Myeloperoxidase Deficiency
Neurosarcoidosis
Polyglandular deficiency syndromes
Primary Sclerosing Cholangitis
Prolactin Promoter Polymorphism
Protein C Deficiency
Protein S Deficiency
Psoriasis
Psoriatic arthritis
Risk of Decreased Metabolism of Thyroid Hormones
Severe Combined Immunodeficiency Syndrome
Severe Combined Immunodeficiency with Sensitivity to Ionizing Radiation
Severe Congenital Neutropenia
Severe Congenital Neutropenia and Cyclic Neutropenia
T Lymphocyte Deficiency
Type 2 X-linked Lymphoproliferative Syndrome
Wegener’s granulomatosis
X-Linkerd Lymphoproliferative (XLP) Syndrome
X-linked Lymphoproliferative Syndrome (XLP)

Inflammations

Behçet’s Disease
Frontal Fibrosing Alopecia
Idiopathic inflammatory myopathy
Inflammatory Bowel Disease (IBD)
Polymyositis
Presence of the HLA-B27 Allele
Sarcoidosis
Scleroderma
Sjogren’s Syndrome

 

Metabolic

Celiac disease
Gluten Intolerance
Glycation
Greater Insulin Sensitivity with Physical Exercise
Lactose intolerance

Metabolic disorders

Fetuin-A

Methylation

MTHFR 1298 mutation (rs1801131)
MTHFR 677 mutation (rs1801133)

Muscular system

Myasthenia Grave

Neurodegenerative diseases

Charcot-Marie Disease
Louis-Bar Syndrome (Ataxia Telangiectasia)
Multiple sclerosis
Systemic Sclerosis

Respiratory system

Chronic obstructive pulmonary disease

Skeletal system (bones)

Arthritis
Carpal tunnel syndrome
Osteoarthritis
Osteoporosis
Rheumatoid arthritis
Risk of amputation in case of diabetic foot ulcer

Skin

Alopecia Areata
Generalized Vitiligo
Rosacea
Vitiligo

Urinary system

Membranoproliferative Glomerulonephritis (GNMP)
Nephrotic syndrome

Vision (Ophthalmology)

Diabetic retinopathy