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Metadata
ID	GENO:0000930
Name	digenic inheritance
Parent Relationships	is_a multifactorial inheritance
Related Diseases	has material basis in proteasome-associated autoinflammatory syndrome 1 methylmalonic aciduria and homocystinuria type cblC hereditary hypophosphatemic rickets with hypercalciuria spinocerebellar ataxia type 17 Parkinson's disease 6 craniosynostosis 7 proteasome-associated autoinflammatory syndrome 3 facioscapulohumeral muscular dystrophy 3 facioscapulohumeral muscular dystrophy 4 oculocutaneous albinism type IB digenic disease AMED syndrome ocular albinism with sensorineural deafness short-rib thoracic dysplasia 7 with or without polydactyly retinitis pigmentosa 7 autosomal recessive nonsyndromic deafness 1A long QT syndrome 1 long QT syndrome 2 long QT syndrome 3 long QT syndrome 5 long QT syndrome 6 long QT syndrome 9 Usher syndrome type 1D Usher syndrome type 2C Waardenburg syndrome type 2A Joubert syndrome 15 Joubert syndrome 9 facioscapulohumeral muscular dystrophy 2 autosomal-mitochondrial sensorineural deafness iminoglycinuria hereditary coproporphyria primary pulmonary hypertension dyskeratosis congenita acrocallosal syndrome