X-linked monogenic disease +
pigmentation disease +

46,XY sex reversal 2
Abruzzo-Erickson syndrome
acanthosis nigricans
Bloch-Sulzberger syndrome
cataract 40
congenital bilateral absence of vas deferens +
conjunctival pigmentation
corpus callosum agenesis-abnormal genitalia syndrome
developmental and epileptic encephalopathy 90
dilated cardiomyopathy 3B
Dowling-Degos disease
dyschromatosis symmetrica hereditaria
dyschromatosis universalis hereditaria
fetal akinesia deformation sequence syndrome X-linked
hyperpigmentation of eyelid
hypopigmentation of eyelid
McLeod syndrome
Meester-Loeys syndrome
Melnick-Needles syndrome
neonatal jaundice +
non-syndromic X-linked intellectual disability +
Ogden syndrome
ovarian dysgenesis 2
primary ovarian insufficiency 1
primary ovarian insufficiency 4
reducing body myopathy 1B
reticulate acropigmentation of Kitamura
retinitis pigmentosa 2
retinitis pigmentosa 24
split hand-foot malformation 2
stromal corneal pigmentation
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 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 nonsyndromic deafness +
X-linked panhypopituitarism
X-linked recessive disease +
X-linked retinitis pigmentosa and sinorespiratory infections
X-linked thrombophilia due to factor IX defect