OBSOLETE: Atrichia-intellectual disability and growth delay syndrome
ORPHA:1211OBSOLETE: Cataract-intellectual disability-anal atresia-urinary defects syndrome
ORPHA:1381OBSOLETE: Congenital muscular dystrophy-muscle hypertrophy-severe intellectual disability syndrome
ORPHA:329206OBSOLETE: Cranioacrofacial syndrome
ORPHA:1339OBSOLETE: Dwarfism-intellectual disability-eye abnormality syndrome
ORPHA:2650OBSOLETE: Genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
ORPHA:330197OBSOLETE: Hirsutism-skeletal dysplasia-intellectual disability syndrome
ORPHA:2156OBSOLETE: Intellectual disability-cataracts-kyphosis syndrome
ORPHA:171860OBSOLETE: Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
ORPHA:404440OBSOLETE: Intellectual disability-hypotonia-skin hyperpigmentation syndrome
ORPHA:3050OBSOLETE: Intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome
ORPHA:3067OBSOLETE: Intellectual disability-microcephaly-unusual facies syndrome
ORPHA:3313OBSOLETE: Intellectual disability-unusual facies syndrome
ORPHA:3043OBSOLETE: Intellectual disability-unusual facies, Davis-Lafer type
ORPHA:3046OBSOLETE: McLain-Dekaban syndrome
ORPHA:2474OBSOLETE: MECP2 duplication syndrome
ORPHA:85281OBSOLETE: Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
ORPHA:102284OBSOLETE: Myopathy-growth delay-intellectual disability-hypospadias syndrome
ORPHA:2601OBSOLETE: Osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome
ORPHA:91133OBSOLETE: Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3
ORPHA:261512OBSOLETE: Short stature-heart defect-craniofacial anomalies syndrome
ORPHA:1088OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome
ORPHA:2580OBSOLETE: Spondylocostal dysostosis-hypospadias-intellectual disability syndrome
ORPHA:329252OBSOLETE: 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:2920Ophthalmological abnormalities-facial dysmorphism-intellectual disability syndrome
ORPHA:698090Optic atrophy-intellectual disability syndrome
ORPHA:401777Osteopenia-intellectual disability-sparse hair syndrome
ORPHA:2324Pachygyria-intellectual disability-epilepsy syndrome
ORPHA:2798Pinsky-Di George-Harley syndrome
ORPHA:2895Preaxial polydactyly-colobomata-intellectual disability syndrome
ORPHA:2921Proximal Xq28 duplication syndrome
ORPHA:1762Pseudo-TORCH syndrome type 1
ORPHA:1229Pseudoprogeria syndrome
ORPHA:2985Pterygium colli-intellectual disability-digital anomalies syndrome
ORPHA:2988Ramos-Arroyo syndrome
ORPHA:1051Rare genetic syndromic intellectual disability
ORPHA:183763Rare non-syndromic intellectual disability
ORPHA:101685