lissencephaly +
X-linked monogenic disease +

46,XY sex reversal 2
Abruzzo-Erickson syndrome
cataract 40
congenital bilateral absence of vas deferens +
corpus callosum agenesis-abnormal genitalia syndrome
developmental and epileptic encephalopathy 90
dilated cardiomyopathy 3B
fetal akinesia deformation sequence syndrome X-linked
lissencephaly 1
lissencephaly 10
lissencephaly 3
lissencephaly 5
lissencephaly 7 with cerebellar hypoplasia
lissencephaly 8
lissencephaly 9 with complex brainstem malformation
McLeod syndrome
Meester-Loeys syndrome
Melnick-Needles syndrome
microlissencephaly +
non-syndromic X-linked intellectual disability +
Norman-Roberts syndrome
Ogden syndrome
ovarian dysgenesis 2
pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
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 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 1
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