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Metadata
ID	GENO:0000146
Name	X-linked dominant inheritance
Synonyms	X-linked dominant inheritance [EXACT]
Parent Relationships	is_a X-linked inheritance
Related Diseases	has material basis in Danon disease X-linked hypophosphatemic rickets orofaciodigital syndrome I X-linked endothelial corneal dystrophy Lisch epithelial corneal dystrophy chromosome Xp11.23-p11.22 duplication syndrome Nance-Horan syndrome Christianson syndrome developmental and epileptic encephalopathy 9 Holoprosencephaly 13, X-linked female-restricted Wieacker-Wolff syndrome congenital disorder of glycosylation type IIm developmental and epileptic encephalopathy 85 X-linked dominant disease reducing body myopathy 1A X-linked chondrodysplasia punctata 2 developmental and epileptic encephalopathy 2 developmental and epileptic encephalopathy 36 Cornelia de Lange syndrome 2 Cornelia de Lange syndrome 5 primary ovarian insufficiency 2A alpha thalassemia-X-linked intellectual disability syndrome X-linked Alport syndrome amelogenesis imperfecta type 1E Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked dominant 1 neurodegeneration with brain iron accumulation 5 46,XX sex reversal 1 46,XX sex reversal 3 otopalatodigital syndrome type 1 otopalatodigital syndrome type 2 congenital nystagmus 5 linear skin defects with multiple congenital anomalies 1 syndromic microphthalmia 2 CHILD syndrome nonphotosensitive trichothiodystrophy 5 linear skin defects with multiple congenital anomalies 3 linear skin defects with multiple congenital anomalies 2 non-syndromic X-linked intellectual disability 2 non-syndromic X-linked intellectual disability 19 female-restricted syndromic X-linked intellectual disability 99 non-syndromic X-linked intellectual disability 89 non-syndromic X-linked intellectual disability 1 non-syndromic X-linked intellectual disability 91 non-syndromic X-linked intellectual disability 98 non-syndromic X-linked intellectual disability 63 non-syndromic X-linked intellectual disability 107 non-syndromic X-linked intellectual disability 41 Raynaud-Claes syndrome chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia deafness, dystonia, and cerebral hypomyelination fragile X syndrome craniofrontonasal syndrome focal dermal hypoplasia Coffin-Lowry syndrome