Informaţii despre

Nume Hidradenitis Suppurativa
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Hidradenitis suppurativa
Clasificare anatomică Malacards Boli de piele

Vezi şi

Boli A-Z Acne Inversa, Familial, 1 Acne Inversa, Familial, 2, with or Without Dowling-Degos Disease Acne Inversa, Familial, 3 Actinomycosis Adenocarcinoma Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Alzheimer Disease 3 Amyloidosis Anal Canal Squamous Cell Carcinoma Anal Fistula Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Anterior Cutaneous Nerve Entrapment Syndrome Anus Cancer Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Back Pain Basal Cell Carcinoma, Infundibulocystic Blau Syndrome Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Breast Squamous Cell Carcinoma Cellulitis Cholesteatoma Chorioretinitis Chronic Pain Colitis Crohn's Colitis Crohn's Disease Cutaneous Candidiasis Dent Disease 1 Dent Disease 2 Dermatitis Diabetes Mellitus Diarrhea Dowling-Degos Disease Down Syndrome Elephantiasis Endotheliitis Epidermodysplasia Verruciformis Epidermolysis Bullosa Simplex Epidermolysis Bullosa Simplex, Dowling-Meara Type Epidermolysis Bullosa Simplex with Mottled Pigmentation Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form Fanconi Anemia, Complementation Group E Filamentary Keratitis Folliculitis Fox-Fordyce Disease Galactose Epimerase Deficiency Granulomatous Dermatitis Granulomatous Mastitis Hantavirus Pulmonary Syndrome Hereditary Spherocytosis Hidradenitis Hinman Syndrome Histiocytosis Ileitis Ileocolitis Inflammatory Bowel Disease Inflammatory Bowel Disease 1 Interstitial Keratitis Keratitis, Hereditary Keratoacanthoma Keratosis Langerhans Cell Histiocytosis Large Cell Acanthoma Lissencephaly 1 Lymphadenitis Lymphangioma Lymphedema Malignant Atrophic Papulosis Mastitis Melanoma Melkersson-Rosenthal Syndrome Mucinous Adenocarcinoma Mycobacterium Chelonae Mycobacterium Tuberculosis 1 Myocardial Infarction Nephrotic Syndrome Neurofibromatosis, Type Ii Neuropathy Ocular Toxoplasmosis Osteomyelitis Perifolliculitis Capitis Abscedens Et Suffodiens, Familial Peripheral Artery Disease Pilonidal Sinus Polycystic Ovary Syndrome Primary Cutaneous Plasmacytosis Pseudoangiomatous Stromal Hyperplasia Psoriasis Psoriasis 13 Pyoderma Pyoderma Gangrenosum Pyoderma Gangrenosum-Acne-Suppurative Hidradenitis Syndrome Reactive Arthritis Reflex Sympathetic Dystrophy Rheumatoid Lung Disease Rosacea Sapho Syndrome Sarcoidosis 1 Sebaceous Gland Disease Sinusitis Skin Disease Spastic Ataxia, Charlevoix-Saguenay Type Spherocytosis, Type 1 Spondylarthropathy Spondylitis Spondyloarthropathy Spondyloarthropathy 1 Spondylocostal Dysostosis 5 Squamous Cell Carcinoma Steatocystoma Multiplex Steatocystoma Multiplex with Natal Teeth Striate Palmoplantar Keratoderma Sweat Gland Disease Teeth Present at Birth Thyroiditis Trichosporonosis Tufted Hair Folliculitis Ulcerative Colitis Urethritis Uveitis White Sponge Nevus 1