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Metadata
ID	GENO:0000936
Name	X-linked inheritance
Parent Relationships	is_a allosomal inheritance
Related Diseases	has material basis in X-linked nonsyndromic deafness X-linked monogenic disease non-syndromic X-linked intellectual disability Ogden syndrome X-linked hereditary ataxia congenital nonspherocytic hemolytic anemia 1 syndromic X-linked intellectual disability X-linked cleft palate with or without ankyloglossia developmental and epileptic encephalopathy 90 X-linked spermatogenic failure 4 X-linked spermatogenic failure 5 X-linked spermatogenic failure 6 X-linked spermatogenic failure 8 ovarian dysgenesis 2 reducing body myopathy 1B primary ovarian insufficiency 1 primary ovarian insufficiency 4 fetal akinesia deformation sequence syndrome X-linked X-linked central diabetes insipidus X-linked mental retardation Gustavson type split hand-foot malformation 2 cataract 40 retinitis pigmentosa 2 retinitis pigmentosa 24 X-linked dilated cardiomyopathy X-linked hypoparathyroidism X-linked exudative vitreoretinopathy 2 X-linked cardiac valvular dysplasia 46,XY sex reversal 2 X-linked panhypopituitarism TARP syndrome Melnick-Needles syndrome syndromic microphthalmia 1 syndromic microphthalmia 13 Abruzzo-Erickson syndrome X-linked reticulate pigmentary disorder Meester-Loeys syndrome congenital bilateral absence of vas deferens X-linked thrombophilia due to factor IX defect McLeod syndrome X-linked epilepsy with variable learning disabilities and behavior disorders X-linked retinitis pigmentosa and sinorespiratory infections Stocco Dos Santos type X-linked intellectual disability corpus callosum agenesis-abnormal genitalia syndrome X-linked lissencephaly 2 X-linked lissencephaly 1