Focal epilepsy-intellectual disability-cerebro-cerebellar malformation
ORPHA:35258712q14 microdeletion syndrome
ORPHA:940632q37 microdeletion syndrome
ORPHA:10013-methylglutaconic aciduria type 9
ORPHA:5052163p25.3 microdeletion syndrome
ORPHA:435638ADNP-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:2850Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome
ORPHA:1014Alpha-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:356996Anophthalmia-heart and pulmonary anomalies-intellectual disability syndrome
ORPHA:91129Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome
ORPHA:1110Aplastic anemia-intellectual disability-dwarfism syndrome
ORPHA:611216Arachnodactyly-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 cerebellar ataxia-epilepsy-intellectual disability syndrome
ORPHA:404481Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency
ORPHA:404499Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency
ORPHA:404493Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency
ORPHA:284282Autosomal recessive distal osteolysis syndrome
ORPHA:2776Autosomal recessive non-syndromic intellectual disability
ORPHA:88616Aymé-Gripp syndrome
ORPHA:1272Birk-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, SBBYS type
ORPHA:3047Blepharophimosis-intellectual disability syndrome, Verloes type
ORPHA:293725Borjeson-Forssman-Lehmann syndrome
ORPHA:127Brachydactyly-mesomelia-intellectual disability-heart defects syndrome
ORPHA:1277CAMOS syndrome
ORPHA:83472Cataract-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:90103CLCN4-related X-linked intellectual disability syndrome
ORPHA:485350Cleft palate-congenital heart defect-intellectual disability syndrome
ORPHA:652519CNTNAP2-related developmental and epileptic encephalopathy
ORPHA:163681Congenital muscular dystrophy with intellectual disability and severe epilepsy
ORPHA:329178