X-linked monogenic disease +
myopathy +

46,XY sex reversal 2
Abruzzo-Erickson syndrome
cataract 40
congenital bilateral absence of vas deferens +
congenital myopathy +
corpus callosum agenesis-abnormal genitalia syndrome
developmental and epileptic encephalopathy 90
dilated cardiomyopathy 3B
fetal akinesia deformation sequence syndrome X-linked
GNE myopathy
King Denborough syndrome
McLeod syndrome
Meester-Loeys syndrome
Melnick-Needles syndrome
mitochondrial myopathy +
muscular atrophy
muscular dystrophy +
myofascial pain syndrome
myofibrillar myopathy +
myoglobinuria
myopathy of extraocular muscle
myopathy with extrapyramidal signs
myositis +
neurogenic scapuloperoneal syndrome Kaeser type
non-syndromic X-linked intellectual disability +
oculopharyngodistal myopathy +
Ogden syndrome
ovarian dysgenesis 2
primary ovarian insufficiency 1
primary ovarian insufficiency 4
reducing body myopathy 1A
retinitis pigmentosa 2
retinitis pigmentosa 24
rhabdomyolysis-myalgia syndrome
split hand-foot malformation 2
syndromic microphthalmia 1
syndromic microphthalmia 13
syndromic X-linked intellectual disability +
TARP syndrome
tubular aggregate myopathy 1
tubular aggregate myopathy 2
X-linked cardiac valvular dysplasia
X-linked central diabetes insipidus
X-linked cleft palate with or without ankyloglossia
X-linked dilated cardiomyopathy
X-linked dominant disease +
X-linked epilepsy with variable learning disabilities and behavior disorders
X-linked exudative vitreoretinopathy 2
X-linked hereditary ataxia +
X-linked hypoparathyroidism
X-linked lissencephaly 1
X-linked lissencephaly 2
X-linked myopathy with excessive autophagy
X-linked nonsyndromic deafness +
X-linked panhypopituitarism
X-linked recessive disease +
X-linked reticulate pigmentary disorder
X-linked retinitis pigmentosa and sinorespiratory infections
X-linked thrombophilia due to factor IX defect