| Name |
|---|
CMD1K Genecardiomyopathy, dilated 1K (autosomal dominant) |
CMD1H Genecardiomyopathy, dilated 1H (autosomal dominant) |
CMD1F Genecardiomyopathy, dilated 1F (autosomal dominant) |
CMD1B Genecardiomyopathy, dilated 1B (autosomal dominant) |
CMD1Q Genecardiomyopathy, dilated 1Q (autosomal dominant) |
EIG4 GeneEpilepsy, idiopathic generalized, susceptibility to 4 |
NPHS2 Genenephrosis 2, idiopathic, steroid-resistant (podocin) This gene encodes a protein that plays a role in the regulation of glomerular permeability. Mutations in this gene cause steroid-resistant nephrotic syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
EIG3 GeneEpilepsy, idiopathic generalized, susceptibility to 3 |
EIG2 GeneEpilepsy, idiopathic generalized, susceptibility to 2 |
EIG5 GeneEpilepsy, idiopathic generalized, susceptibility to, 5 |
IPOX GeneIntestinal pseudoobstruction, neuronal, primary idiopathic |
IS2 GeneScoliosis, idiopathic 2 |
IS1 GeneAdolescent idiopathic scoliosis |
IS5 Genescoliosis, idiopathic, susceptibility to, 5 |
IS4 GeneScoliosis, idiopathic, susceptibility to, 4 |
IBGC1 Geneidiopathic basal ganglia calcification 1 |
IBGC2 GeneBasal ganglia calcification, idiopathic, 2 |
EGI Geneepilepsy, generalized, idiopathic |