Informaţii despre

Nume Amelogenesis Imperfecta
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Hereditary disturbances in tooth structure, not elsewhere classified
Clasificare anatomică Malacards Boli bucale; Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Amelogenesis Imperfecta Type 2a1; Amelogenesis Imperfecta, Type Ia; Amelogenesis Imperfecta, Type Ib; Amelogenesis Imperfecta, Type Ic; Amelogenesis Imperfecta, Type Ie; Amelogenesis Imperfecta, Type if; Amelogenesis Imperfecta, Type Ig; Amelogenesis Imperfecta, Type Ih; Amelogenesis Imperfecta, Type Iiia; Amelogenesis Imperfecta, Type Iiib; Amelogenesis Imperfecta, Type Iv

Vezi şi

Boli A-Z Aggressive Periodontitis Aland Island Eye Disease Albinism Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Totalis Al-Raqad Syndrome Amelogenesis Imperfecta Hypomaturation Type Amelogenesis Imperfecta, Hypoplastic/hypomaturation, X-Linked 2 Amelogenesis Imperfecta Hypoplastic Type, Ig Amelogenesis Imperfecta Local Hypoplastic Amelogenesis Imperfecta, Type Ib Amelogenesis Imperfecta, Type Ie Amelogenesis Imperfecta, Type Iiia Amelogenesis Imperfecta, Type Iv Androgen Insensitivity Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autoimmune Inner Ear Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brachyolmia Cataract 5, Multiple Types Cerebral Palsy, Ataxic, Autosomal Recessive Cleft Lip Dementia Dental Fluorosis Dental Pulp Calcification Dental Pulp Necrosis Dentin Dysplasia Dentinogenesis Imperfecta Ectodermal Dysplasia Enamel Caries Encephalopathy Epidermolysis Bullosa Epilepsy Epulis Fibromatosis Freemartinism Gingival Fibromatosis Gingival Overgrowth Gingivitis Growth Hormone Deficiency Hair Whorl Hypocalcified Amelogenesis Imperfecta Hypoplastic Amelogenesis Imperfecta Jalili Syndrome Junctional Epidermolysis Bullosa Kohlschutter-Tonz Syndrome Leber Congenital Amaurosis 4 Linear Skin Defects with Multiple Congenital Anomalies 1 Microphthalmia Nephrocalcinosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Neurofibromatosis, Type Iv, of Riccardi Oculocutaneous Albinism Osteopetrosis Periodontitis Phelan-Mcdermid Syndrome Polycystic Kidney Disease Pseudoxanthoma Elasticum Renal Tubular Acidosis Retinitis Pigmentosa 59 Root Resorption Salt and Pepper Developmental Regression Syndrome Scoliosis, Isolated 1 Sensorineural Hearing Loss Skeletal Dysplasias Split Foot Split Hand Spondyloenchondrodysplasia Taurodontism Teeth Hard Tissue Disease Tetraamelia Syndrome, Autosomal Recessive Trichodentoosseous Syndrome Verloes Bourguignon Syndrome