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Boli A-Z 9q22.3 Microdeletion Acanthoma Acquired Immunodeficiency Syndrome Acral Lentiginous Melanoma Acrokeratosis Verruciformis Actinic Keratosis Acute Lymphocytic Leukemia Adenocarcinoma Adenoid Basal Cell Carcinoma Adenoiditis Adenoma Adie Pupil Adult Xanthogranuloma Aging Albinism Alopecia Universalis Congenita Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Ameloblastoma Amyloidosis Anaplastic Large Cell Lymphoma Androgen Insensitivity, Partial Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Aplasia Cutis Congenita Apocrine Adenoma Arthrochalasia Ehlers-Danlos Syndrome Astrocytoma Basal Cell Carcinoma Basal Cell Carcinoma 2 Basal Cell Carcinoma 3 Basal Cell Carcinoma 4 Basal Cell Carcinoma 5 Basal Cell Carcinoma 6 Basal Cell Carcinoma 7 Basal Cell Carcinoma, Infundibulocystic Basal Cell Carcinoma, Multiple Basal Cell Nevus Syndrome Basaloid Follicular Hamartoma Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant Basaloid Squamous Cell Carcinoma Basosquamous Carcinoma Bazex Syndrome Benign Mesenchymoma Blepharitis Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bloom Syndrome Bornholm Eye Disease Breast Cancer Brooke-Spiegler Syndrome Bullous Pemphigoid Burns Burn Scar Capillary Malformations, Congenital Cardiomyopathy, Familial Restrictive, 1 Cartilage-Hair Hypoplasia Cell Type Benign Neoplasm Cell Type Cancer Cerebellar Medulloblastoma Cervicitis Childhood Medulloblastoma Chronic Enteropathy Associated with Slco2a1 Gene Chronic Maxillary Sinusitis Chronic Ulcer of Skin Chylomicron Retention Disease Clear Cell Basal Cell Carcinoma Cleft Lip Cloacogenic Carcinoma Conotruncal Heart Malformations Cortisone Reductase Deficiency 1 Cryptococcosis Cutaneous Adenocystic Carcinoma Cutaneous Leishmaniasis Cyanosis, Transient Neonatal Cystadenoma Cystic Basal Cell Carcinoma Cytochrome P450 2d6 Variant Demodicidosis Dermatitis Dermatofibrosarcoma Protuberans Dyskeratosis Congenita, X-Linked Ectropion Empty Sella Syndrome Endotheliitis Eosinophilic Pustular Folliculitis Epidermoid Cysts Epidermolysis Bullosa Epidermolytic Hyperkeratosis Epilepsy Epithelial Recurrent Erosion Dystrophy Erysipelas Exophthalmos Eyelid Neoplasm Fanconi Anemia, Complementation Group E Fibroepithelial Basal Cell Carcinoma Fibrosarcoma Focal Dermal Hypoplasia Folliculitis Glioblastoma Glioblastoma Multiforme Granuloma Annulare Heart Cancer Hemangioma Hemochromatosis, Type 1 Hepatic Adenomas, Familial Hereditary Leiomyomatosis and Renal Cell Cancer Hidradenoma Hidrocystoma Histiocytosis Histoplasmosis Hyperinsulinemic Hypoglycemia, Familial, 6 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Scars Hypohidrosis Hypomelanotic Disorder Hypotrichosis Hypotrichosis 1 Hypoxia Ichthyosis Indeterminate Cell Histiocytosis Infiltrative Basal Cell Carcinoma Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Irritant Dermatitis Keloids Keratoacanthoma Keratocystic Odontogenic Tumor Keratosis Large Cell Carcinoma Learning Disability Leiomyomatosis Leiomyosarcoma Leishmaniasis Lentigines Lentigo Maligna Melanoma Leukemia Leukoplakia Lichen Planus Lichen Sclerosus Lymphadenitis Lymphedema Lymphoepithelioma-Like Carcinoma Lymphoma Lymphomatoid Papulosis Malaria, Mild Marshall-Smith Syndrome Maxillary Sinusitis Mediastinitis Medulloblastoma Melanoma Meningioma, Familial Meningothelial Meningioma Merkel Cell Carcinoma Mesenchymoma Metatypical Basal Cell Carcinoma Micronodular Basal Cell Carcinoma Migraine with or Without Aura 1 Miyoshi Muscular Dystrophy 1 Molluscum Contagiosum Morpheaform Basal Cell Carcinoma Muir-Torre Syndrome Multiple Acyl-Coa Dehydrogenase Deficiency Multiple Familial Trichoepithelioma Multiple Mitochondrial Dysfunctions Syndrome 5 Myelophthisic Anemia Myiasis Myoclonic-Astastic Epilepsy Myoclonus, Familial Cortical Myotonic Dystrophy Neurodegeneration with Brain Iron Accumulation 2a Neurofibroma Neurofibromatosis, Type I Neurofibromatosis, Type Ii Neurofibromatosis, Type Iv, of Riccardi Neuroma Neuronitis Neuropathy Neutrophil Actin Dysfunction Nevus Comedonicus Nevus, Epidermal Nodular Basal Cell Carcinoma Oculocutaneous Albinism Odontogenic Myxoma Oral Leukoplakia Ovarian Fibroma Paget Disease, Extramammary Pancreatic Cancer Pancreatitis Papilledema Papilloma Parkinsonism with Spasticity, X-Linked Pemphigus Pemphigus Vulgaris Penis Basal Cell Carcinoma Persistent Idiopathic Facial Pain Phacomatosis Pigmentokeratotica Phaeohyphomycosis Pheochromocytoma Pigmented Basal Cell Carcinoma Pilar Sheath Acanthoma Pilocytic Astrocytoma Pilomatrix Carcinoma Pilomatrixoma Pityriasis Rubra Pilaris Pleomorphic Adenoma Porokeratosis Posttransplant Acute Limbic Encephalitis Primary Cutaneous Anaplastic Large Cell Lymphoma Primary Cutaneous Follicle Center Lymphoma Prostatitis Psoriasis Psoriasis 13 Psoriasis 5 Pulmonary Alveolar Microlithiasis Pure Red-Cell Aplasia Pyogenic Granuloma Recessive Dystrophic Epidermolysis Bullosa Refsum Disease, Classic Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome Retinal Vein Occlusion Retinitis Rhabdomyomatous Mesenchymal Hamartoma Rickets Rombo Syndrome Rosacea Sarcoma Sarcomatoid Basal Cell Carcinoma Sarcomatoid Squamous Cell Skin Carcinoma Scabies Schimmelpenning-Feuerstein-Mims Syndrome Schizoaffective Disorder Scrotum Basal Cell Carcinoma Short-Rib Thoracic Dysplasia 9 with or Without Polydactyly Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sinusitis Situs Inversus Skin Benign Neoplasm Skin Disease Skin/hair/eye Pigmentation, Variation in, 5 Skin Squamous Cell Carcinoma Skin Tag Small Cell Carcinoma Smallpox Spastic Ataxia, Charlevoix-Saguenay Type Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spindle Cell Carcinoma Spiradenoma Spondylolisthesis Spondyloocular Syndrome Squamous Cell Carcinoma Sturge-Weber Syndrome Superficial Basal Cell Carcinoma Superficial Spreading Melanoma Syringocystadenoma Papilliferum Syringoma Temporal Arteritis Teratoma Testicular Thecoma Thyroiditis Tinea Capitis Tinea Corporis Tinea Pedis Trichofolliculoma Trigeminal Trophic Syndrome Turner Syndrome Urticaria Uruguay Faciocardiomusculoskeletal Syndrome Vaginitis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Vulva Basal Cell Carcinoma Vulvar Basal Cell Carcinoma Weber Syndrome West Syndrome Xeroderma Pigmentosum, Complementation Group C