CDC/NIH Web Information Database

---

Last data update: Sep 09, 2024. (Total: 8777 Documents)

All Cancer Diabetes Economic Environmental Equity FHH HLBS ID Implementation ND PGx PI Rare RCH dataset

All CDC NIH

Next

Records 1-30 (of 37 Records)

CDC/NIH Web Information
Study finds genetic basis for drug response in childhood absence epilepsy NIH Press Release, April 11, 2017
Pachygyria-intellectual disability-epilepsy syndrome From NCATS Genetic and Rare Diseases Information Center
Alopecia epilepsy oligophrenia syndrome of Moynahan From NCATS Genetic and Rare Diseases Information Center
Alopecia, epilepsy, pyorrhea, mental subnormality From NCATS Genetic and Rare Diseases Information Center
Benign familial infantile epilepsy From NCATS Genetic and Rare Diseases Information Center
Benign familial neonatal epilepsy From NCATS Genetic and Rare Diseases Information Center
Epilepsy juvenile absence From NCATS Genetic and Rare Diseases Information Center
Epilepsy mental deterioration Finnish type From NCATS Genetic and Rare Diseases Information Center
Epilepsy occipital calcifications From NCATS Genetic and Rare Diseases Information Center
Epilepsy progressive myoclonic type 3 From NCATS Genetic and Rare Diseases Information Center
Epilepsy telangiectasia From NCATS Genetic and Rare Diseases Information Center
Myoclonic astatic epilepsy From NCATS Genetic and Rare Diseases Information Center
Epilepsy, benign occipital From NCATS Genetic and Rare Diseases Information Center
Epilepsy, partial, familial From NCATS Genetic and Rare Diseases Information Center
Autosomal dominant partial epilepsy with auditory features From NCATS Genetic and Rare Diseases Information Center
Genetic reflex epilepsy From NCATS Genetic and Rare Diseases Information Center
Infant epilepsy with migrant focal crisis From NCATS Genetic and Rare Diseases Information Center
Northern epilepsy From NCATS Genetic and Rare Diseases Information Center
Spastic paraplegia-epilepsy-intellectual disability syndrome From NCATS Genetic and Rare Diseases Information Center
Temporal epilepsy, familial From NCATS Genetic and Rare Diseases Information Center
Photosensitive epilepsy From NCATS Genetic and Rare Diseases Information Center
Juvenile myoclonic epilepsy From NCATS Genetic and Rare Diseases Information Center
Progressive myoclonic epilepsy From NCATS Genetic and Rare Diseases Information Center
Myoclonus epilepsy From NCATS Genetic and Rare Diseases Information Center
Myoclonus epilepsy partial seizure From NCATS Genetic and Rare Diseases Information Center
Myoclonic epilepsy with ragged red fibers From NCATS Genetic and Rare Diseases Information Center
Post-traumatic epilepsy From NCATS Genetic and Rare Diseases Information Center
Pyridoxine-dependent epilepsy From NCATS Genetic and Rare Diseases Information Center
Myokymia with neonatal epilepsy From NCATS Genetic and Rare Diseases Information Center
Benign rolandic epilepsy (BRE) From NCATS Genetic and Rare Diseases Information Center