X-linked dominant disease +
myopathy +

46,XX sex reversal 1
46,XX sex reversal 3
alpha thalassemia-X-linked intellectual disability syndrome
amelogenesis imperfecta type 1E
Charcot-Marie-Tooth disease X-linked dominant 1
Charcot-Marie-Tooth disease X-linked dominant 6
CHILD syndrome
Christianson syndrome
chromosome Xp11.23-p11.22 duplication syndrome
Coffin-Lowry syndrome
congenital disorder of glycosylation type IIm
congenital myopathy +
congenital nystagmus 5
Cornelia de Lange syndrome 2
Cornelia de Lange syndrome 5
craniofrontonasal syndrome
Danon disease
deafness, dystonia, and cerebral hypomyelination
developmental and epileptic encephalopathy 2
developmental and epileptic encephalopathy 36
developmental and epileptic encephalopathy 85
developmental and epileptic encephalopathy 9
female-restricted syndromic X-linked intellectual disability 99
focal dermal hypoplasia
fragile X syndrome
GNE myopathy
King Denborough syndrome
linear skin defects with multiple congenital anomalies 1
linear skin defects with multiple congenital anomalies 2
linear skin defects with multiple congenital anomalies 3
Lisch epithelial corneal dystrophy
mitochondrial myopathy +
muscular atrophy
muscular dystrophy +
myofascial pain syndrome
myofibrillar myopathy +
myoglobinuria
myopathy of extraocular muscle
myopathy with extrapyramidal signs
myositis +
Nance-Horan syndrome
neurodegeneration with brain iron accumulation 5
neurogenic scapuloperoneal syndrome Kaeser type
non-syndromic X-linked intellectual disability 1
non-syndromic X-linked intellectual disability 107
non-syndromic X-linked intellectual disability 19
non-syndromic X-linked intellectual disability 2
non-syndromic X-linked intellectual disability 41
non-syndromic X-linked intellectual disability 63
non-syndromic X-linked intellectual disability 89
non-syndromic X-linked intellectual disability 91
non-syndromic X-linked intellectual disability 98
nonphotosensitive trichothiodystrophy 5
oculopharyngodistal myopathy +
orofaciodigital syndrome I
otopalatodigital syndrome type 1
otopalatodigital syndrome type 2
primary ovarian insufficiency 2A
Raynaud-Claes syndrome
reducing body myopathy 1B
rhabdomyolysis-myalgia syndrome
syndromic microphthalmia 2
tubular aggregate myopathy 1
tubular aggregate myopathy 2
X-linked Alport syndrome
X-linked chondrodysplasia punctata 2 +
X-linked dominant hypophosphatemic rickets
X-linked endothelial corneal dystrophy
X-linked myopathy with excessive autophagy