Developmental delay

Code	`248290002`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20020131

12288440021p35.2 microdeletion syndrome disorder

7196520072p21 microdeletion syndrome disorder

718221007Behr syndrome disorder

238047006Beta-D-mannosidosis disorder

720565000Bohring Opitz syndrome disorder

720606005Cardiocranial syndrome Pfeiffer type disorder

425805004Cognitive developmental delay disorder

773648002Congenital cataract, hearing loss, severe developmental delay syndrome disorder

773398005Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome disorder

1197059004Congenital ichthyosis, microcephalus, tetraplegia syndrome disorder

721088003DEND syndrome disorder

123526007Delay in sexual development AND/OR puberty disorder

229740001Delayed pre-verbal development disorder

426881004Developmental delay in feeding disorder

703478008Developmental delay in social skills disorder

1340174002Developmental delay, immunodeficiency, leucoencephalopathy, hypohomocysteinemia syndrome disorder

733521003Distal 16p11.2 microdeletion syndrome disorder

1366590005Early-onset neurodegeneration, choreoathetoid movement, microcytic anaemia due to IREB2 mutation disorder

1172593006Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome disorder

229734008Expressive language delay disorder

720958002Frank-Ter Haar syndrome disorder

1281842000GNAO1-related developmental delay, seizures, movement disorder spectrum disorder

224958001Global developmental delay disorder

1303868000Intermediate DEND syndrome disorder

1216940001Joint contractures, developmental delay, Pierre Robin syndrome disorder

1300133004KLHL7-related Bohring Opitz-like syndrome disorder

717338006Koolen De Vries syndrome disorder

778026007Lethal polymalformative syndrome Boissel type disorder

1234819007Limb girdle muscular dystrophy due to POMK deficiency disorder

1237514002Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome disorder

760491000000102Motor developmental delay disorder

1137472008Neurodevelopmental delay disorder

1373563007Neuronal ceroid lipofuscinosis type 1 disorder

1373771009Neuronal ceroid lipofuscinosis type 5 disorder

722051004Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome disorder

1255268002Oculocerebrodental syndrome disorder

774071007Pancytopenia with developmental delay syndrome disorder

229718005Phonological delay disorder

718227006Proximal 16p11.2 microdeletion syndrome disorder

229736005Receptive language delay disorder

874931001Severe achondroplasia, developmental delay, acanthosis nigricans syndrome disorder

1187212004Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome disorder

1360070001Spastic paraparesis, cataracts, speech delay syndrome disorder

229721007Speech delay disorder

733066002Trigonocephaly, short stature, developmental delay syndrome disorder

719833004Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome disorder

782877002Xp22.13p22.2 duplication syndrome disorder

Parents (1)

Children (47)