HSD10 disease, atypical type
ORPHA:8529512q14 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-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:356996Aplastic anemia-intellectual disability-dwarfism syndrome
ORPHA:611216Arachnodactyly-abnormal ossification-intellectual disability syndrome
ORPHA:1129Ataxia-deafness-intellectual disability syndrome
ORPHA:1188Atkin-Flaitz syndrome
ORPHA:1193Autosomal dominant non-syndromic intellectual disability
ORPHA:178469Autosomal recessive chorioretinopathy-microcephaly syndrome
ORPHA:2518Autosomal recessive distal osteolysis syndrome
ORPHA:2776Birk-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:293725CAMOS syndrome
ORPHA:83472Cardiocranial syndrome, Pfeiffer type
ORPHA:2872Cataract-hypertrichosis-intellectual disability syndrome
ORPHA:1375Cataract-intellectual disability-hypogonadism syndrome
ORPHA:1387CHAMP1-related intellectual disability-facial dysmorphism-behavioral abnormalities syndrome
ORPHA:692193Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome
ORPHA:90103CK syndrome
ORPHA:251383CLCN4-related X-linked intellectual disability syndrome
ORPHA:485350Cortical blindness-intellectual disability-polydactyly syndrome
ORPHA:1389Craniodigital-intellectual disability syndrome
ORPHA:1514Craniosynostosis-microretrognathia-severe intellectual disability syndrome
ORPHA:565858Cutis 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:369891Digital anomalies-intellectual disability-short stature syndrome
ORPHA:352487DYRK1A-related intellectual disability syndrome
ORPHA:464306GMS syndrome
ORPHA:2090Growth delay due to insulin-like growth factor type 1 deficiency
ORPHA:73272Growth delay-intellectual disability-hepatopathy syndrome
ORPHA:541423Hennekam syndrome
ORPHA:2136Hepatic fibrosis-renal cysts-intellectual disability syndrome
ORPHA:2031Hernández-Aguirre Negrete syndrome
ORPHA:2139