Vezi şi

Boli A-Z Abdominal Wall Defect Acanthoma Acute Monoblastic Leukemia Adenocarcinoma Aging Ainhum Albinism Alopecia Alopecia, Androgenetic, 1 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Aminoaciduria Amyloidosis Anhidrosis Aniridia 1 Anorexia Nervosa 1 Anosmia Anterior Cutaneous Nerve Entrapment Syndrome Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Attention Deficit-Hyperactivity Disorder Autism Autism X-Linked 2 Autosomal Dominant Progressive External Ophthalmoplegia Autosomal Recessive Congenital Ichthyosis Basal Cell Carcinoma Bazex Syndrome Biliary Atresia Blau Syndrome Blepharoconjunctivitis Blood Group--Ahonen 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 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brachydactyly Branchiootic Syndrome 1 Burns Candidiasis Cataract Cellulitis Cerebellar Degeneration Cerebellar Hypoplasia Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome Cerebritis Cerebro-Oculo-Facio-Skeletal Syndrome Cervical Rib Cervicitis Chanarin-Dorfman Syndrome Cholangitis Cholestasis Chondrodysplasia Punctata 2, X-Linked Dominant Chondrodysplasia Punctata Syndrome Chromosome Xp Deletion Chronic Mucocutaneous Candidiasis Cicatricial Ectropion Clear Cell Acanthoma Coats Disease Compartment Syndrome Congenital Disorder of Glycosylation, Type Iq Congenital Hypothyroidism Congenital Ichthyosiform Erythroderma Constrictive Pericarditis Corneal Degeneration Corneal Disease Corneal Dystrophy Corneal Neovascularization Cryoglobulinemia Cutaneous Candidiasis Cutaneous Mastocytosis Cutis Laxa Cutis Laxa, Autosomal Recessive, Type Iiia Cystinuria Dermatitis Dermatitis, Atopic, 2 Dermatophytosis Dermotrichic Syndrome Diffuse Cutaneous Mastocytosis Diffuse Idiopathic Skeletal Hyperostosis Distal Arthrogryposis Dominant Ichthyosis Vulgaris Down Syndrome Dwarfism Dysferlinopathy Dystonia Ectodermal Dysplasia Ectropion Eczema Herpeticum Endodermal Sinus Tumor Endometrial Adenocarcinoma End Stage Renal Failure Eosinophilic Fasciitis Epidermodysplasia Verruciformis Epidermolysis Bullosa Epidermolysis Bullosa Simplex Epidermolytic Acanthoma Epidermolytic Hyperkeratosis Epidermolytic Nevus Epilepsy Erythroderma, Ichthyosiform, Congenital Reticular Exfoliative Ichthyosis Exocrine Pancreatic Insufficiency Fanconi Syndrome Fasciitis Filamentary Keratitis Fragile X Syndrome Glomerulonephritis Granuloma Annulare Growth Hormone Deficiency Hansen's Disease Helix Syndrome Hepatic Adenomas, Familial Hepatitis Histiocytosis Holocarboxylase Synthetase Deficiency Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperostosis Hyperparathyroidism Hypertrichosis Hypertrophic Pyloric Stenosis Hypoglycemia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypohidrosis Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypotrichosis Ichthyosiform Erythroderma, Corneal Involvement, and Deafness Ichthyosis, Acquired Ichthyosis Bullosa of Siemens Ichthyosis--Cheek--Eyebrow Syndrome Ichthyosis, Congenital, Autosomal Recessive 1 Ichthyosis, Congenital, Autosomal Recessive 11 Ichthyosis, Congenital, Autosomal Recessive 2 Ichthyosis, Congenital, Autosomal Recessive 4a Ichthyosis, Congenital, Autosomal Recessive 4b Ichthyosis, Congenital, Autosomal Recessive 7 Ichthyosis Congenita with Biliary Atresia Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis Ichthyosis, Follicular Ichthyosis, Hepatosplenomegaly, and Cerebellar Degeneration Ichthyosis Hystrix, Curth-Macklin Type Ichthyosis Hystrix Gravior Ichthyosis Lamellar 2 Ichthyosis Lamellar 3 Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis Ichthyosis Linearis Circumflexa Ichthyosis Prematurity Syndrome Ichthyosis Vulgaris Ichthyosis, X-Linked Ifap Syndrome with or Without Bresheck Syndrome Inflammatory Linear Verrucous Epidermal Nevus Inguinal Hernia Ischemia Juvenile Rheumatoid Arthritis Kagami-Ogata Syndrome Kallmann Syndrome Kaufman Oculocerebrofacial Syndrome Keratitis, Hereditary Keratosis Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Kid Syndrome Leber Congenital Amaurosis Leber Congenital Amaurosis 5 Lelis Syndrome Leukemia Lichen Amyloidosis Lichen Planus Lipid Metabolism Disorder Lipid Storage Disease Lipodystrophy Liver Disease Lung Cancer Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphangiectasis Lymphatic Malformations Lymphoblastic Leukemia Lymphoma Lymphomatoid Papulosis Malignant Histiocytosis Melanoma Microcephaly Muckle-Wells Syndrome Multiple Sulfatase Deficiency Muscular Dystrophy Myoclonus Myopathy Nail Disorder, Nonsyndromic Congenital, 1 Nephrotic Syndrome Netherton Syndrome Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Ii Neuronitis Neuropathy Nevoid Hypermelanosis, Linear and Whorled Ocular Albinism Ocular Motor Apraxia Oral Squamous Cell Carcinoma Pachyonychia Congenita 1 Palmoplantar Keratoderma, Nonepidermolytic Palmoplantar Keratosis Pancreatitis Papilloma Parapsoriasis Peeling Skin Syndrome Pellucid Marginal Degeneration Pericarditis Perifolliculitis Capitis Abscedens Et Suffodiens, Familial Peripheral T-Cell Lymphoma Phelan-Mcdermid Syndrome Pityriasis Lichenoides Pityriasis Lichenoides Chronica Pityriasis Rotunda Pityriasis Rubra Pilaris Pneumonia Poems Syndrome Polyneuropathy Pre-Descemet Corneal Dystrophy Prostatitis Pseudoainhum Psoriasis Psoriasis 13 Pulmonary Alveolar Microlithiasis Pycnodysostosis Pyle Disease Pyloric Stenosis Quadriplegia Recessive Dystrophic Epidermolysis Bullosa Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome Retinitis Retinitis Pigmentosa Rhabdomyosarcoma Rheumatoid Arthritis Rickets Rud Syndrome Sclerosing Cholangitis Self-Improving Collodion Baby Sensorineural Hearing Loss Shwachman-Diamond Syndrome Sjogren-Larsson Syndrome Skin Conditions Skin Disease Spastic Diplegia Spasticity Spastic Quadriplegia Squamous Cell Carcinoma Steatorrhea Sveinsson Chorioretinal Atrophy Systemic Lupus Erythematosus Testicular Microlithiasis Testicular Yolk Sac Tumor Three M Syndrome 1 Thyroiditis Tinea Corporis Transitional Cell Carcinoma Transmitted_by Ventricular Septal Defect Vohwinkel Syndrome Vohwinkel Syndrome, Variant Form Wells Syndrome White Sponge Nevus 1