Congenital muscular dystrophy with intellectual disability
ORPHA:370968Congenital muscular dystrophy with intellectual disability and severe epilepsy
ORPHA:3291782q37 microdeletion syndrome
ORPHA:1001Allan-Herndon-Dudley syndrome
ORPHA:59Alopecia-contractures-dwarfism-intellectual disability syndrome
ORPHA:1005Alopecia-intellectual disability syndrome
ORPHA:2850Aniridia-cerebellar ataxia-intellectual disability syndrome
ORPHA:1065Aniridia-intellectual disability syndrome
ORPHA:1068Aplastic 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:2776Autosomal recessive non-syndromic intellectual disability
ORPHA:88616Autosomal recessive proximal renal tubular acidosis
ORPHA:93607Aymé-Gripp syndrome
ORPHA:1272Birk-Barel syndrome
ORPHA:166108Blepharophimosis-intellectual disability syndrome
ORPHA:293642Blepharophimosis-intellectual disability syndrome, MKB type
ORPHA:293707Blepharophimosis-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:90103CLCN4-related X-linked intellectual disability syndrome
ORPHA:485350Congenital insensitivity to pain with severe intellectual disability
ORPHA:453510Congenital muscular dystrophy without intellectual disability
ORPHA:370980Cortical blindness-intellectual disability-polydactyly syndrome
ORPHA:1389Craniodigital-intellectual disability syndrome
ORPHA:1514Cryptorchidism-arachnodactyly-intellectual disability syndrome
ORPHA:1548Cutis verticis gyrata-intellectual disability syndrome
ORPHA:1557De 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:2983DNMT3A-related microcephalic dwarfism
ORPHA:658595DYRK1A-related intellectual disability syndrome
ORPHA:464306Dysequilibrium syndrome
ORPHA:1766Early-onset parkinsonism-intellectual disability syndrome
ORPHA:2379EGF-related primary hypomagnesemia with intellectual disability
ORPHA:620368Fallot complex-intellectual disability-growth delay syndrome
ORPHA:3304Female restricted epilepsy with intellectual disability
ORPHA:101039Filippi syndrome
ORPHA:3255FRAXE intellectual disability
ORPHA:100973Growth delay due to insulin-like growth factor type 1 deficiency
ORPHA:73272Growth delay-intellectual disability-hepatopathy syndrome
ORPHA:541423Hair defect-photosensitivity-intellectual disability syndrome
ORPHA:1408