Lujan-Fryns syndrome
ORPHA:776Allan-Herndon-Dudley syndrome
ORPHA:59Alopecia-contractures-dwarfism-intellectual disability syndrome
ORPHA:1005Atkin-Flaitz syndrome
ORPHA:1193CK syndrome
ORPHA:251383CLCN4-related X-linked intellectual disability syndrome
ORPHA:485350Congenital insensitivity to pain with severe intellectual disability
ORPHA:453510Congenital muscular dystrophy with intellectual disability
ORPHA:370968Congenital muscular dystrophy with intellectual disability and severe epilepsy
ORPHA:329178Congenital muscular dystrophy without intellectual disability
ORPHA:370980Deafness-intellectual disability syndrome, Martin-Probst type
ORPHA:85321EGF-related primary hypomagnesemia with intellectual disability
ORPHA:620368Female restricted epilepsy with intellectual disability
ORPHA:101039FRAXE intellectual disability
ORPHA:100973HSD10 disease, atypical type
ORPHA:85295Intellectual disability, Wolff type
ORPHA:3080Kahrizi syndrome
ORPHA:168972KDM5C-related syndromic X-linked intellectual disability
ORPHA:85279Marfanoid habitus-autosomal recessive intellectual disability syndrome
ORPHA:2463Mietens syndrome
ORPHA:2557Multiple congenital anomalies/dysmorphic syndrome without intellectual disability
ORPHA:102285NKAP-related intellectual disability-facial dysmorphism-marfanoid habitus-scoliosis syndrome
ORPHA:700325OBSOLETE: MECP2 duplication syndrome
ORPHA:85281OBSOLETE: Non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature
ORPHA:371064OBSOLETE: Syndromic neurometabolic disease with non-X-linked intellectual disability
ORPHA:182073OBSOLETE: Syndromic neurometabolic disease with X-linked intellectual disability
ORPHA:182076OBSOLETE: X-linked congenital disorder of glycosylation with intellectual disability as a major feature
ORPHA:371054OBSOLETE: X-linked dominant intellectual disability-epilepsy syndrome
ORPHA:93951OBSOLETE: X-linked intellectual disability-obesity-short stature syndrome
ORPHA:85331OBSOLETE: X-linked intellectual disability-precocious puberty-obesity syndrome
ORPHA:85318OBSOLETE: X-linked intellectual disability, Martinez type
ORPHA:775OBSOLETE: X-linked intellectual disability, Raynaud type
ORPHA:3061OBSOLETE: X-linked intellectual disability, Schutz type
ORPHA:3062OBSOLETE: X-linked intellectual disability, Wittner type
ORPHA:3064Partington syndrome
ORPHA:94083Proximal Xq28 duplication syndrome
ORPHA:1762Rare genetic intellectual disability
ORPHA:183757Rare intellectual disability
ORPHA:87277Renpenning syndrome
ORPHA:3242Severe X-linked intellectual disability, Gustavson type
ORPHA:3078Syndromic X-linked intellectual disability 7
ORPHA:85274Vasquez-Hurst-Sotos syndrome
ORPHA:3423Wilson-Turner syndrome
ORPHA:3459X-linked alpha-thalassemia-intellectual disability syndrome
ORPHA:847X-linked cerebral-cerebellar-coloboma syndrome
ORPHA:163961X-linked intellectual disability due to GRIA3 mutations
ORPHA:364028X-linked intellectual disability with isolated growth hormone deficiency
ORPHA:67045X-linked intellectual disability-acromegaly-hyperactivity syndrome
ORPHA:85327