ICD-10: R62

Lack of expected normal physiological development in childhood and adults

Coding Guidelines

Excludes 1

  • delayed puberty (E30.0)
  • hypopituitarism (E23.0)
  • gonadal dysgenesis (Q99.1)

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obsolete physical disorder OBSOLETED TERM X-linked dominant hypophosphatemic rickets Alstrom syndrome congenital disorder of glycosylation type II acrocapitofemoral dysplasia Allan-Herndon-Dudley syndrome anauxetic dysplasia 1 atelosteogenesis alcohol-related birth defects spastic cerebral palsy Athabaskan brainstem dysgenesis syndrome adolescence-adult electroclinical syndrome Meckel syndrome obsolete Opitz-GBBB syndrome iridogoniodysgenesis syndrome tarsal-carpal coalition syndrome Perrault syndrome pancreatic agenesis Koolen de Vries syndrome IMAGe syndrome autism spectrum disorder acrofrontofacionasal dysostosis Adams-Oliver syndrome Baraitser-Winter syndrome Van Maldergem syndrome synpolydactyly Smith-McCort dysplasia Simpson-Golabi-Behmel syndrome type 1 sclerosteosis renal-hepatic-pancreatic dysplasia pontocerebellar hypoplasia pontocerebellar hypoplasia type 2B pontocerebellar hypoplasia type 2C pontocerebellar hypoplasia type 5 pontocerebellar hypoplasia type 6 Ohdo syndrome syndromic X-linked intellectual disability acromelic frontonasal dysostosis microcephaly with or without chorioretinopathy, lymphedema, or mental retardation acrofacial dysostosis Cincinnati type mandibulofacial dysostosis with alopecia Hennekam syndrome orofaciodigital syndrome III orofaciodigital syndrome IV Joubert syndrome with orofaciodigital defect orofaciodigital syndrome XI acrofacial dysostosis Rodriguez type chromosome 14q11-q22 deletion syndrome chromosome 16p12.1 deletion syndrome chromosome 2q31.2 deletion syndrome chromosome 3q29 microdeletion syndrome chromosome 6q24-q25 deletion syndrome chromosome 16p13.3 duplication syndrome chromosome 17p13.3 duplication syndrome chromosome 17q21.31 duplication syndrome chromosome 22q13 duplication syndrome Cole-Carpenter syndrome chromosome 5p13 duplication syndrome fetal valproate syndrome Goldberg-Shprintzen syndrome EAST syndrome Mowat-Wilson syndrome Barber-Say syndrome lethal congenital contracture syndrome 1 lethal congenital contracture syndrome 2 Char syndrome Ritscher-Schinzel syndrome Ritscher-Schinzel syndrome 2 3MC syndrome 2 XFE progeroid syndrome obsolete anterior segment mesenchymal dysgenesis chondrodysplasia-pseudohermaphroditism syndrome lethal congenital contracture syndrome 4 autosomal recessive Robinow syndrome autosomal dominant Robinow syndrome 3 hypomyelinating leukodystrophy 13 syndromic X-linked intellectual disability Lubs type syndromic X-linked intellectual disability 17 syndromic X-linked intellectual disability 7 syndromic X-linked intellectual disability Abidi type syndromic X-linked intellectual disability Chudley-Schwartz type syndromic X-linked intellectual disability 14 autosomal recessive pseudohypoaldosteronism type 1

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