Wilson-Turner syndrome
ORPHA:345912q14 microdeletion syndrome
ORPHA:940632q37 microdeletion syndrome
ORPHA:1001Allan-Herndon-Dudley syndrome
ORPHA:59Alopecia-contractures-dwarfism-intellectual disability syndrome
ORPHA:1005Alopecia-epilepsy-pyorrhea-intellectual disability syndrome
ORPHA:1008Alopecia-intellectual disability syndrome
ORPHA:2850Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
ORPHA:98791Aniridia-cerebellar ataxia-intellectual disability syndrome
ORPHA:1065Aniridia-intellectual disability syndrome
ORPHA:1068Aniridia-ptosis-intellectual disability-familial obesity syndrome
ORPHA:1067ANK3-related intellectual disability-sleep disturbance syndrome
ORPHA:356996Aplastic anemia-intellectual disability-dwarfism syndrome
ORPHA:611216Arachnodactyly-intellectual disability-dysmorphism syndrome
ORPHA:1130Ataxia-deafness-intellectual disability syndrome
ORPHA:1188Atkin-Flaitz syndrome
ORPHA:1193Autosomal dominant non-syndromic intellectual disability
ORPHA:178469Autosomal recessive distal osteolysis syndrome
ORPHA:2776Birk-Barel syndrome
ORPHA:166108Blepharophimosis-intellectual disability syndrome
ORPHA:293642Blepharophimosis-intellectual disability syndrome, MKB type
ORPHA:293707Blepharophimosis-intellectual disability syndrome, Ohdo type
ORPHA:2728Blepharophimosis-intellectual disability syndrome, Verloes type
ORPHA:293725Borjeson-Forssman-Lehmann syndrome
ORPHA:127Cataract-hypertrichosis-intellectual disability syndrome
ORPHA:1375Cataract-intellectual disability-hypogonadism syndrome
ORPHA:1387Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome
ORPHA:90103CK syndrome
ORPHA:251383CLCN4-related X-linked intellectual disability syndrome
ORPHA:485350Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome
ORPHA:363741Craniodigital-intellectual disability syndrome
ORPHA:1514Cutis verticis gyrata-intellectual disability syndrome
ORPHA:1557Cutis verticis gyrata-thyroid aplasia-intellectual disability syndrome
ORPHA:79482De Barsy syndrome
ORPHA:2962Deafness-intellectual disability syndrome, Martin-Probst type
ORPHA:85321Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
ORPHA:369891Difference of sex development-intellectual disability syndrome
ORPHA:2983Digital anomalies-intellectual disability-short stature syndrome
ORPHA:352487DNMT3A-related microcephalic dwarfism
ORPHA:658595DOORS syndrome
ORPHA:79500DYRK1A-related intellectual disability syndrome
ORPHA:464306Early-onset parkinsonism-intellectual disability syndrome
ORPHA:2379Fallot complex-intellectual disability-growth delay syndrome
ORPHA:3304Filippi syndrome
ORPHA:3255GMS syndrome
ORPHA:2090GNB5-related intellectual disability-cardiac arrhythmia syndrome
ORPHA:542306Growth delay due to insulin-like growth factor type 1 deficiency
ORPHA:73272Growth delay-intellectual disability-hepatopathy syndrome
ORPHA:541423