Myhre syndrome
ORPHA:258812q14 microdeletion syndrome
ORPHA:940632q37 microdeletion syndrome
ORPHA:1001AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome
ORPHA:412069Allan-Herndon-Dudley syndrome
ORPHA:59Alopecia-contractures-dwarfism-intellectual disability syndrome
ORPHA:1005Alopecia-intellectual disability syndrome
ORPHA:2850Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome
ORPHA:1014Aniridia-intellectual disability syndrome
ORPHA:1068Aniridia-ptosis-intellectual disability-familial obesity syndrome
ORPHA:1067Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome
ORPHA:1110Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome
ORPHA:324540Aplastic anemia-intellectual disability-dwarfism syndrome
ORPHA:611216Arachnodactyly-intellectual disability-dysmorphism syndrome
ORPHA:1130Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome
ORPHA:3145Ataxia-deafness-intellectual disability syndrome
ORPHA:1188Autosomal dominant intellectual disability-craniofacial dysmorphism-macrocephaly-hypotonia syndrome due to H1-4 mutation
ORPHA:642763Autosomal recessive distal osteolysis syndrome
ORPHA:2776Aymé-Gripp syndrome
ORPHA:1272Birk-Barel syndrome
ORPHA:166108Blepharophimosis-intellectual disability syndrome
ORPHA:293642Blepharophimosis-intellectual disability syndrome, MKB type
ORPHA:293707Blepharophimosis-intellectual disability syndrome, SBBYS type
ORPHA:3047Blepharophimosis-intellectual disability syndrome, Verloes type
ORPHA:293725BPTF-related intellectual disability-facial dysmorphism-skeletal anomalies syndrome
ORPHA:686482Brain abnormalities-severe developmental delay-facial dysmorphism-intellectual disability syndrome
ORPHA:664410Brain abnormalities-severe developmental delay-facial dysmorphism-intellectual disability syndrome due to MEF2C mutation
ORPHA:664416Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome due to TAB2 mutation
ORPHA:664401Cataract-intellectual disability-hypogonadism syndrome
ORPHA:1387CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome
ORPHA:600668CDK13-related developmental delay-intellectual disability-facial dysmorphism-congenital heart defects syndrome
ORPHA:646278CHAMP1-related intellectual disability-facial dysmorphism-behavioral abnormalities syndrome
ORPHA:692193Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome
ORPHA:90103CHD3-related developmental delay-speech delay-intellectual disability-abnormalities of vision-facial dysmorphism syndrome
ORPHA:599082CHD8 overgrowth syndrome
ORPHA:642675CLCN4-related X-linked intellectual disability syndrome
ORPHA:485350Cono-spondylar dysplasia
ORPHA:420794Cortical blindness-intellectual disability-polydactyly syndrome
ORPHA:1389Craniodigital-intellectual disability syndrome
ORPHA:1514Craniofacial dysmorphism-skeletal anomalies-intellectual disability syndrome
ORPHA:228407Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome
ORPHA:459061Cryptorchidism-arachnodactyly-intellectual disability syndrome
ORPHA:1548Cutaneous mastocytosis-deafness-microtia syndrome
ORPHA:2135Cutis verticis gyrata-intellectual disability syndrome
ORPHA:1557Deafness-epiphyseal dysplasia-short stature syndrome
ORPHA:3218Deafness-intellectual disability syndrome, Martin-Probst type
ORPHA:85321Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome
ORPHA:71267