OBSOLETE: Grix-Blankenship-Peterson syndrome
ORPHA:209912q14 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: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-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 recessive distal osteolysis syndrome
ORPHA:2776Aymé-Gripp syndrome
ORPHA:1272Birk-Barel syndrome
ORPHA:166108Blepharophimosis-intellectual disability syndrome
ORPHA:293642Blepharophimosis-intellectual disability syndrome, Ohdo type
ORPHA:2728BPTF-related intellectual disability-facial dysmorphism-skeletal anomalies syndrome
ORPHA:686482Brachydactyly-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:1387CDK13-related developmental delay-intellectual disability-facial dysmorphism-congenital heart defects syndrome
ORPHA:646278Charcot-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:652519Craniodigital-intellectual disability syndrome
ORPHA:1514Craniofacial dysmorphism-skeletal anomalies-intellectual disability syndrome
ORPHA:228407Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome
ORPHA:459061Craniosynostosis-microretrognathia-severe intellectual disability syndrome
ORPHA:565858Cryptorchidism-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:2983Digital anomalies-intellectual disability-short stature syndrome
ORPHA:352487DOORS syndrome
ORPHA:79500DYRK1A-related intellectual disability syndrome
ORPHA:464306Dysequilibrium syndrome
ORPHA:1766