OBSOLETE: Syndromic neurometabolic disease with non-X-linked intellectual disability
ORPHA:182073OBSOLETE: Syndromic neurometabolic disease with X-linked intellectual disability
ORPHA:182076OBSOLETE: Trichodermal syndrome-intellectual disability syndrome
ORPHA:3360OBSOLETE: 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:3064OBSOLETE: X-linked recessive intellectual disability-macrocephaly-ciliary dysfunction syndrome
ORPHA:83648Oliver syndrome
ORPHA:2920Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome
ORPHA:2743Optic atrophy-intellectual disability syndrome
ORPHA:401777Partington syndrome
ORPHA:94083Pinsky-Di George-Harley syndrome
ORPHA:2895POMT1-related limb-girdle muscular dystrophy R11
ORPHA:86812Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome
ORPHA:477673Premature chromosome condensation with microcephaly and intellectual disability
ORPHA:52183Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome
ORPHA:391408Proximal Xq28 duplication syndrome
ORPHA:1762Pseudo-TORCH syndrome type 1
ORPHA:1229Rare genetic syndromic intellectual disability
ORPHA:183763Rare non-syndromic intellectual disability
ORPHA:101685Rare syndromic intellectual disability
ORPHA:102369Renpenning syndrome
ORPHA:3242SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome
ORPHA:597743Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome
ORPHA:397933Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome
ORPHA:1236Severe X-linked intellectual disability, Gustavson type
ORPHA:3078Spastic paraplegia-glaucoma-intellectual disability syndrome
ORPHA:2818Syndromic X-linked intellectual disability 7
ORPHA:85274Tall stature-intellectual disability-renal anomalies syndrome
ORPHA:500095Thumb stiffness-brachydactyly-intellectual disability syndrome
ORPHA:1078Trichomegaly-retina pigmentary degeneration-dwarfism syndrome
ORPHA:3363Ulna hypoplasia-intellectual disability syndrome
ORPHA:2249Vasquez-Hurst-Sotos syndrome
ORPHA:3423White-Sutton syndrome
ORPHA:468678Wilson-Turner syndrome
ORPHA:3459Witteveen-Kolk syndrome
ORPHA:500163X-linked alpha-thalassemia-intellectual disability syndrome
ORPHA:847X-linked cerebral-cerebellar-coloboma syndrome
ORPHA:163961X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome
ORPHA:431140X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability
ORPHA:480880X-linked intellectual disability due to GRIA3 mutations
ORPHA:364028X-linked intellectual disability-acromegaly-hyperactivity syndrome
ORPHA:85327X-linked intellectual disability-ataxia-apraxia syndrome
ORPHA:85338X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome
ORPHA:324410