Kahrizi syndrome
ORPHA:16897212q14 microdeletion syndrome
ORPHA:940632q37 microdeletion syndrome
ORPHA:1001ADNP-related blepharophimosis-intellectual disability syndrome
ORPHA:700160Allan-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:98791Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818Aniridia-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:356996Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome
ORPHA:1110Aplastic anemia-intellectual disability-dwarfism syndrome
ORPHA:611216Arachnodactyly-abnormal ossification-intellectual disability syndrome
ORPHA:1129Arachnodactyly-intellectual disability-dysmorphism syndrome
ORPHA:1130Ataxia-deafness-intellectual disability syndrome
ORPHA:1188Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome
ORPHA:370022Autosomal dominant non-syndromic intellectual disability
ORPHA:178469Autosomal recessive distal osteolysis syndrome
ORPHA:2776Autosomal recessive non-syndromic intellectual disability
ORPHA:88616Autosomal recessive spastic paraplegia type 11
ORPHA:2822Aymé-Gripp syndrome
ORPHA:1272Birk-Barel syndrome
ORPHA:166108Blepharophimosis-intellectual disability syndrome
ORPHA:293642Blepharophimosis-intellectual disability syndrome due to UBE3B deficiency
ORPHA:329255Blepharophimosis-intellectual disability syndrome, MKB type
ORPHA:293707Blepharophimosis-intellectual disability syndrome, Ohdo type
ORPHA:2728Blepharophimosis-intellectual disability syndrome, SBBYS type
ORPHA:3047Blepharophimosis-intellectual disability syndrome, Verloes type
ORPHA:293725Blepharophimosis-intellectual disability syndrome/genitopatellar overlap syndrome
ORPHA:597746Borjeson-Forssman-Lehmann syndrome
ORPHA:127Brachydactyly-mesomelia-intellectual disability-heart defects syndrome
ORPHA:1277Cardiocranial syndrome, Pfeiffer type
ORPHA:2872Cataract-combined malonic and methylmalonic aciduria-intellectual disability syndrome
ORPHA:699835Cataract-hypertrichosis-intellectual disability syndrome
ORPHA:1375Cataract-intellectual disability-hypogonadism syndrome
ORPHA:1387Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome
ORPHA:90103CHIME syndrome
ORPHA:3474CLCN4-related X-linked intellectual disability syndrome
ORPHA:485350Cleft palate-congenital heart defect-intellectual disability syndrome
ORPHA:652519Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome
ORPHA:363741Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome
ORPHA:352333Congenital muscular dystrophy with intellectual disability
ORPHA:370968Congenital muscular dystrophy-cataract-intellectual disability syndrome
ORPHA:662184Cooper-Jabs syndrome
ORPHA:1488