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Hidradenitis
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Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)
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
Anhidrosis
Aniridia 1
Annular Erythema
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 Granulomatous Disease
Chronic Pain
Colitis
Crohn's Colitis
Crohn's Disease
Cutaneous Candidiasis
Dent Disease 1
Dent Disease 2
Diabetes Mellitus
Diarrhea
Dowling-Degos Disease
Down Syndrome
Elephantiasis
Endocarditis
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
Hidradenitis Suppurativa
Hinman Syndrome
Histiocytosis
Hydrops, Lactic Acidosis, and Sideroblastic Anemia
Ileitis
Ileocolitis
Inflammatory Bowel Disease
Inflammatory Bowel Disease 1
Interstitial Keratitis
Keratoacanthoma
Keratosis
Langerhans Cell Histiocytosis
Large Cell Acanthoma
Leukemia
Lissencephaly 1
Lung Cancer
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
Orbital Cellulitis
Osteomyelitis
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial
Peripheral Artery Disease
Pilonidal Sinus
Polycystic Ovary Syndrome
Polydactyly, Postaxial, Type A1
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
Sialadenitis
Sinusitis
Skin Disease
Spastic Ataxia, Charlevoix-Saguenay Type
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
Vasculitis
White Sponge Nevus 1
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