Disease Index
9,486 diseasesX-linked immunoneurologic disorder
X-linked immunoneurologic disorder is characterized by immune deficiency and neurological disorders in females, and by neonatal death in males
MeSH: C536743
X-linked intellectual disability
syndromic intellectual characterized by an X-linked inheritance pattern
MeSH: D038901
X-linked intellectual disability with isolated growth hormone deficiency
human disease
X-linked intellectual disability-acromegaly-hyperactivity syndrome
X-linked intellectual disability-ataxia-apraxia syndrome
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome
Human disease
X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome
human disease
X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome
X-linked intellectual disability-craniofacioskeletal syndrome
human disease
MeSH: C567471
X-linked intellectual disability-cubitus valgus-dysmorphism syndrome
, mild microcephaly, a short philtrum, deep-set eyes, downslanting palpebral fissures and multiple nevi. Less than ten individuals have been described so far. Transmission is thought to be X-linked recessive.
MeSH: C564510
X-linked intellectual disability-epilepsy syndrome
human disease
X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome
X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome
human disease
X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome
X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome
MeSH: C536715
X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome
X-linked intellectual disability-hypotonia-movement disorder syndrome
human disease
X-linked intellectual disability-hypotonic face syndrome
Mental retardation-hypotonic facies covers a group of X-linked syndromes characterized by severe intellectual deficit and facial dysmorphism, with variable other features
X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome
#945;-fetoprotein and intrauterine growth restriction is observed in routine pregnancy examination
X-linked intellectual disability-macrocephaly-macroorchidism syndrome
disease
X-linked intellectual disability-plagiocephaly syndrome
disease
MeSH: C537512
X-linked intellectual disability-precocious puberty-obesity syndrome
X-linked intellectual disability-psychosis-macroorchidism syndrome
syndromic X-linked intellectual disability characterized by moderate intellectual deficit, manic-depressive psychosis, pyramidal signs and macroorchidism that has material basis in mutation in the MECP2 gene on chromosome Xq28
X-linked intellectual disability-seizures-psoriasis syndrome
X-linked intellectual disability-seizures-psoriasis syndrome has been described in four male cousins. The mode of inheritance is thought to be X-linked recessive.
MeSH: C536978
X-linked intellectual disability-short stature-overweight syndrome
X-linked intellectual disability-spastic quadriparesis syndrome
human disease
MeSH: C564099
X-linked intellectual disability, Cilliers type
X-linked intellectual disability, Golabi-Ito-hall type
X-linked intellectual disability, Pai type
X-linked intellectual disability, Porteous type
human disease