Deafness-intellectual disability syndrome, Martin-Probst type
ORPHA:8532112q14 microdeletion syndrome
ORPHA:940632q37 microdeletion syndrome
ORPHA:10013p25.3 microdeletion syndrome
ORPHA:435638Allan-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:1067Anophthalmia-heart and pulmonary anomalies-intellectual disability syndrome
ORPHA:91129Anterior maxillary protrusion-strabismus-intellectual disability syndrome
ORPHA:562559Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome
ORPHA:324540Aplastic anemia-intellectual disability-dwarfism syndrome
ORPHA:611216Ataxia-deafness-intellectual disability syndrome
ORPHA:1188Atkin-Flaitz syndrome
ORPHA:1193Autosomal recessive distal osteolysis syndrome
ORPHA:2776Autosomal recessive spastic paraplegia type 11
ORPHA:2822Aymé-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:1277Cardiocranial syndrome, Pfeiffer type
ORPHA:2872Cataract-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:652519Cleft palate-congenital heart defect-intellectual disability syndrome due to MEIS2 mutation
ORPHA:652514Cortical blindness-intellectual disability-polydactyly syndrome
ORPHA:1389Craniodigital-intellectual disability syndrome
ORPHA:1514Cutis verticis gyrata-intellectual disability syndrome
ORPHA:1557De Barsy syndrome
ORPHA:2962Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Deafness-infertility syndrome
ORPHA:94064Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome
ORPHA:71267Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
ORPHA:369891Difference of sex development-intellectual disability syndrome
ORPHA:2983DNMT3A-related microcephalic dwarfism
ORPHA:658595DOORS syndrome
ORPHA:79500DYRK1A-related intellectual disability syndrome
ORPHA:464306