Informaţii despre

Nume Ectodermal Dysplasia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Ectodermal dysplasia (anhidrotic)

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Boli A-Z Absent Breasts and Nipples Acanthosis Nigricans Achalasia Adult Syndrome Agammaglobulinemia Aggressive Periodontitis Aging Alopecia Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amelogenesis Imperfecta Anhidrosis Aniridia 1 Ankylosis Anodontia Anorexia Nervosa 1 Aredyld Arrhythmogenic Right Ventricular Cardiomyopathy Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Ectodermal Dysplasia, Cleft Lip/palate, and Developmental Delay Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Atrophic Rhinitis Ayme-Gripp Syndrome B-Cell Lymphomas Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brachydactyly Branchiooculofacial Syndrome Breast Cancer Breasts and/or Nipples, Aplasia or Hypoplasia of, 1 Bronchial Disease Buruli Ulcer Bustos Simosa Pinto Cisternas Syndrome Candidiasis Cataract Cataract 5, Multiple Types Chand Syndrome Cherubism Choanal Atresia, Posterior Choroideremia Cleft Lip Cleft Lip and Alveolus Cleft Lip/palate Cleft Lip/palate-Ectodermal Dysplasia Syndrome Clouston Syndrome Colitis Congenital Contractures Congenital Dyserythropoietic Anemia Conjunctivitis Corpus Callosum, Agenesis of, with Abnormal Genitalia Cote Katsantoni Syndrome Cystic Fibrosis Dermatopathia Pigmentosa Reticularis Dermoodontodysplasia Diabetes Mellitus Dilated Cardiomyopathy Distal Arthrogryposis Dwarfism Dyskeratosis Congenita Dysphagia Ectodermal Dysplasia 10a, Hypohidrotic/hair/nail Type, Autosomal Dominant Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive Ectodermal Dysplasia 11a, Hypohidrotic/hair/tooth Type, Autosomal Dominant Ectodermal Dysplasia 11b, Hypohidrotic/hair/tooth Type, Autosomal Recessive Ectodermal Dysplasia 1, Hypohidrotic, X-Linked Ectodermal Dysplasia 4, Hair/nail Type Ectodermal Dysplasia 9, Hair/nail Type Ectodermal Dysplasia, Anhidrotic, with T-Cell Immunodeficiency, Autosomal Dominant Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy Syndrome Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia Ectodermal Dysplasia, Hypohidrotic, with Immune Deficiency Ectodermal Dysplasia/skin Fragility Syndrome Ectodermal Dysplasia-Syndactyly Syndrome 1 Ectodermal Dysplasia-Syndactyly Syndrome 2 Ectodermal Dysplasia with Mental Retardation and Syndactyly Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/palate Syndrome 1 Ectropion Ehlers-Danlos Syndrome Ellis-Van Creveld Syndrome Encephalopathy Evans' Syndrome Fabry Disease Familial Adenomatous Polyposis 1 Fanconi Anemia, Complementation Group E Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly Focal Dermal Hypoplasia Folliculitis Galactose Epimerase Deficiency Gingivitis Hematopoietic Stem Cell Transplantation Hidrotic Ectodermal Dysplasia 2 Holoprosencephaly Hydrocephalus Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hypermobile Ehlers-Danlos Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypohidrosis Hypohidrotic Ectodermal Dysplasia Autosomal Recessive Hypohidrotic Ectodermal Dysplasia with Immunodeficiency Hypopituitarism Hypotrichosis Ichthyosis Incontinentia Pigmenti Isolated Cleft Lip Keloids Keratoacanthoma Keratoconus Keratosis Kid Syndrome Lacrimal Duct Obstruction Lelis Syndrome Leukemia Limbal Stem Cell Deficiency Lipodystrophy, Congenital Generalized, Type 2 Lipoid Proteinosis of Urbach and Wiethe Lutheran Suppressor, X-Linked Lymphedema Lymphoid Interstitial Pneumonia Lymphoma Lymphopenia Martinez Monasterio Pinheiro Syndrome Medulloblastoma Melanoma Microcephaly Microphthalmia Miliary Tuberculosis Myiasis Myopathy Naegeli-Franceschetti-Jadassohn Syndrome Nasopharyngitis Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neutropenia Nevus Comedonicus Nodular Medulloblastoma Odontoonychodermal Dysplasia Oligohydramnios Orchitis Osteopetrosis Otodental Dysplasia Panuveitis Pectus Excavatum Periodontitis Pili Torti Primary Agammaglobulinemia Protein-Losing Enteropathy Ptosis Purpura Rapp-Hodgkin Syndrome Renovascular Hypertension Retinitis Rhabdomyosarcoma Rhinitis Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sickle Cell Disease Solitary Median Maxillary Central Incisor Spastic Ataxia, Charlevoix-Saguenay Type Specific Antibody Deficiency Split Foot Split Hand Spondylocarpotarsal Synostosis Syndrome Squamous Cell Carcinoma Strabismus Sudden Infant Death Syndrome Sveinsson Chorioretinal Atrophy Sweat Gland Disease Taurodontism T Cell Deficiency Telangiectasis Tetralogy of Fallot Tetramelic Deficiencies, Ectodermal Dysplasia, Deformed Ears, and Other Abnormalities Thalassemia Three M Syndrome 1 Thumb Deformity, Alopecia, Pigmentation Anomaly Thymic Dysplasia Tooth Agenesis Tracheal Cancer Transient Hypogammaglobulinemia Trichoscyphodysplasia Trueb Burg Bottani Syndrome Tylosis with Esophageal Cancer Undifferentiated Pleomorphic Sarcoma Uveitis Wells Syndrome Werner Syndrome Zlotogora Syndrome