X-linked monogenic disease +

46,XY sex reversal 2
Abruzzo-Erickson syndrome
cataract 40
congenital bilateral absence of vas deferens +
congenital nonspherocytic hemolytic anemia 1
corpus callosum agenesis-abnormal genitalia syndrome
developmental and epileptic encephalopathy 90
fetal akinesia deformation sequence syndrome X-linked
McLeod syndrome
Meester-Loeys syndrome
Melnick-Needles syndrome
non-syndromic X-linked intellectual disability +
Ogden syndrome
ovarian dysgenesis 2
primary ovarian insufficiency 1
primary ovarian insufficiency 4
reducing body myopathy 1B
retinitis pigmentosa 2
retinitis pigmentosa 24
split hand-foot malformation 2
syndromic microphthalmia 1
syndromic microphthalmia 13
syndromic X-linked intellectual disability +
TARP syndrome
X-linked cardiac valvular dysplasia
X-linked central diabetes insipidus
X-linked cleft palate with or without ankyloglossia
X-linked dilated cardiomyopathy
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 nonsyndromic deafness +
X-linked panhypopituitarism
X-linked recessive disease +
X-linked reticulate pigmentary disorder
X-linked retinitis pigmentosa and sinorespiratory infections
X-linked spermatogenic failure 4
X-linked spermatogenic failure 5
X-linked spermatogenic failure 6
X-linked spermatogenic failure 8
X-linked thrombophilia due to factor IX defect

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 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
female-restricted Wieacker-Wolff syndrome
focal dermal hypoplasia
fragile X syndrome
Holoprosencephaly 13, X-linked
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
Nance-Horan syndrome
neurodegeneration with brain iron accumulation 5
nonphotosensitive trichothiodystrophy 5
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
orofaciodigital syndrome I
otopalatodigital syndrome type 1
otopalatodigital syndrome type 2
primary ovarian insufficiency 2A
Raynaud-Claes syndrome
reducing body myopathy 1A
syndromic microphthalmia 2
X-linked Alport syndrome
X-linked chondrodysplasia punctata 2 +
X-linked dominant hypophosphatemic rickets
X-linked endothelial corneal dystrophy