Disease Index
9,486 diseasesintellectual disability syndrome due to a DYRK1A point mutation
human disease
intellectual disability-balding-patella luxation-acromicria syndrome
intellectual disability-brachydactyly-Pierre robin syndrome
MeSH: C563880
intellectual disability-cataracts-kyphosis syndrome
This syndrome is characterized by severe intellectual deficit, kyphosis with onset in childhood and cataract with onset in late adolescence
intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome
MeSH: C537447
intellectual disability-epilepsy-extrapyramidal syndrome
human disease
intellectual disability-expressive aphasia-facial dysmorphism syndrome
human disease
intellectual disability-facial dysmorphism-hand anomalies syndrome
human disease
intellectual disability-hyperkinetic movement-truncal ataxia syndrome
human disease
intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome
intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome
human disease
intellectual disability-hypotonia-skin hyperpigmentation syndrome
human disease
intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome
human disease
intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome
human disease
intellectual disability-myopathy-short stature-endocrine defect syndrome
MeSH: C535458
intellectual disability-obesity-brain malformations-facial dysmorphism syndrome
intellectual disability-obesity-prognathism-eye and skin anomalies syndrome
human disease
MeSH: C564660
intellectual disability-polydactyly-uncombable hair syndrome
medical condition
MeSH: C537615
intellectual disability-seizures-macrocephaly-obesity syndrome
human disease
intellectual disability-severe speech delay-mild dysmorphism syndrome
intellectual disability-short stature-hypertelorism syndrome
human disease
intellectual disability-spasticity-ectrodactyly syndrome
medical condition
MeSH: C537446
intellectual disability-strabismus syndrome
human disease
intellectual disability, autosomal recessive 53
human disease
intellectual disability, Buenos-Aires type
MeSH: C563095
intellectual disability, Wolff type
MeSH: C537448
intercalary limb defects
human disease
interdigitating dendritic cell sarcoma
histiocytic and dendritic cell cancer that effect dendritic cells
MeSH: D054739
intermediate anorectal malformation
intermediate DEND syndrome