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Hide Details Number of codes found for 'H20': 1

NAICS: 541710   Largest/examples: H20 - H2 - Search H20 - Birth Defects & Genetic Diseases Research

Organizations that conduct research which can be used to improve the prevention, diagnosis and treatment of any of a number of illnesses or conditions that are hereditary and passed from parent to offspring.

Key words: Achronplasia Research; Alagille Syndrome Research; Albinism Research; Amaurotic Familial Idiocy Research; Bardet-Biedl Syndrome Research; Birth Defects Research; Cerebral Palsy Research; Charcot-Marie Disease Research; Charcot-Marie-Tooth Disease Research; Chromosome Disorders Research; Clubfoot Research; Coffin-Lowrey Syndrome Research; Congenital Defects Research; Cri-du-Chat Syndrome Research; Crying Cat Syndrome Research; Cryptorchidism Research; Cystic Fibrosis Research; Cytochrome-c Oxidase Deficiency Research; Dandy-Walker Syndrome Research; De Lange Syndrome Research; Developmental Coordination Disorder Research; Factor X Deficiency Research; Fetal Alcohol Syndrome Research; Fragile X Syndrome Research; Friedreich Ataxia Research; Genetic Diseases Research; Hemophilia Research; Hereditary Diseases Research; Huntingtons Disease Research; Jervell-Lange Nielsen Syndrome Research; Kartagener Syndrome Research; Klinefelter Syndrome Research; Laurence-Moon Syndrome Research; Leigh Disease Research; Lesch-Nyhan Syndrome Research; Littles Disease Research; Lynch Syndrome Research; Marfan Syndrome Research; Martin-Bell Syndrome Research; Mental Retardation Research; Motor Skills Disorder Research; Neurofibromatosis Research; Oral-Facial Clefts Research; Phenylketonuria Research; PKU Research; Porphyria Research; Prader-Willi Syndrome Research; Pseudoxanthoma Elasticum Research; Pyruvate Carboxylase Deficiency Disease Research; Pyruvate Dehydrogenase Complex Deficiency Disease Research; Rett Disorder Research; Rett Syndrome Research; Retts Disorder Research; Retts Syndrome Research; Rett's Disorder Research; Rett's Syndrome Reseach; Rh Disease Research; Romano-Ward Syndrome Research; Rubinstein-Taybi Syndrome Research; Sickle Cell Research; Spina Bifida Research; Sudden Infant Death Research; Tay Sachs Research; Testicular Feminization Syndrome Research; Thalassemia Research; Turner Syndrome Research; Turners Syndrome Research; WAGR Syndrome Research; Werner Syndrome Research; Williams Syndrome Research; Xeroderma Pigmentosum Research