Visualize Submit Comment

Metadata
ID	GENO:0000934
Name	autosomal inheritance
Parent Relationships	is_a monogenic inheritance
Related Diseases	has material basis in familial adenomatous polyposis Weill-Marchesani syndrome Aicardi-Goutieres syndrome autosomal genetic disease Robinow syndrome chromosome 1q41-q42 deletion syndrome septooptic dysplasia combined oxidative phosphorylation deficiency 55 dopamine transporter deficiency syndrome neurodevelopmental disorder with hypotonia and speech delay glucose transporter type 1 deficiency syndrome hereditary spastic paraplegia 30 camptodactyly-tall stature-scoliosis-hearing loss syndrome hereditary desmoid disease exudative vitreoretinopathy 4 Gillespie syndrome congenital nystagmus 1 syndromic microphthalmia 12 syndromic microphthalmia 14 syndromic microphthalmia 8 autosomal hemophilia A thrombophilia due to thrombomodulin defect retinitis pigmentosa 86 distal arthrogryposis type 1C tubulinopathy focal segmental glomerulosclerosis 3 spondylocostal dysostosis 5 hypophosphatasia Sotos syndrome blepharophimosis, ptosis, and epicanthus inversus syndrome McCune Albright syndrome factor XI deficiency familial Mediterranean fever