Talk:International Classification of Diseases

From Embryology

International Classification of Diseases 11

http://apps.who.int/classifications/icd11/browse/f/en

registered 30 July 2012


CDC http://www.cdc.gov/nchs/icd/icd10cm.htm#10update

Australia - ACAMS

Acronym for Australian Congenital Anomalies Monitoring System that monitors Australian data for birth anomalies detected up to 1 year of age. ACAMS superseded the National Congenital Malformations and Birth Defects Data Collection (NCMBD), which commenced in 1981. The equivalent European system is called (eurocat|).
(More? Australian Birth Anomalies System | Australian Statistics]] | Human Abnormal Development | [https://npesu.unsw.edu.au/data-collection/australian-congenital-anomalies-monitoring-system-acams National Perinatal Epidemiology and Statistics Unit)


Europe - eurocat

(EUROCAT) A European network of population-based registries for the epidemiologic surveillance of congenital anomalies. Started in 1979 with more than 1.5 million births surveyed per year in Europe, 43 registries in 20 countries, and 29% of European birth population covered. High quality multiple source registries, ascertaining terminations of pregnancy as well as births.
(More? Human Abnormal Development | eurocat | [http://www.eurocat-network.eu/accessprevalencedata/prevalencetables Prevalence Tables)

USA - NVSS

Acronym for National Vital Statistics System that monitors United States data on births, deaths, marriages, divorces, and fetal deaths.
(More? NVSS | NVSS - Births | NVSS- Fetal Deaths)

The National Center for Health Statistics (NCHS), the Federal agency responsible for use of the International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10) in the United States, has developed a clinical modification of the classification for morbidity purposes. The ICD-10 is used to code and classify mortality data from death certificates, having replaced ICD-9 for this purpose as of January 1, 1999. ICD-10-CM is the replacement for ICD-9-CM, volumes 1 and 2, effective October 1, 2015.

The ICD-10 is copyrighted by the World Health Organization (WHO), which owns and publishes the classification.

http://www.cdc.gov/nchs/nvss.htm

http://www.cdc.gov/nchs/births.htm

http://www.cdc.gov/nchs/fetal_death.htm

ICD-10

Mark Hill (talk) 10:18, 2 April 2019 (AEDT) Deleted ICD-10 information shown below from page

ICD-10 Chapter XVII Congenital malformations, deformations and chromosomal abnormalities

Within ICD-10 classification "congenital malformations, deformations and chromosomal abnormalities" are (Q00-Q99) but excludes "inborn errors of metabolism" (E70-E90).

(ICD) ICD-10 was endorsed by the Forty-third World Health Assembly in May 1990 and came into use in WHO Member States as from 1994. The classification is the latest in a series which has its origins in the 1850s. The first edition, known as the International List of Causes of Death, was adopted by the International Statistical Institute in 1893. WHO took over the responsibility for the ICD at its creation in 1948 when the Sixth Revision, which included causes of morbidity for the first time, was published. The World Health Assembly adopted in 1967 the WHO Nomenclature Regulations that stipulate use of ICD in its most current revision for mortality and morbidity statistics by all Member States.

ICD-10 Links: XVII Congenital Malformations | System Tables | XVI Perinatal Period | XV Pregnancy Childbirth | Abnormal Development | Prenatal Diagnosis | Birth | Neonatal Diagnosis |  ICD-11 | Reports

Congenital malformations of the nervous system (Q00-Q07)

Links: Q00-Q07 Detailed | Neural System - Abnormalities
  • Q00 Anencephaly and similar malformations
  • Q01 Encephalocele Incl.: encephalomyelocele, hydroencephalocele, hydromeningocele, cranial meningocele, cerebral meningoencephalocele Excl.: Meckel-Gruber syndrome (Q61.9)
  • Q02 Microcephaly Incl.: Hydromicrocephaly Micrencephalon Excl.: Meckel-Gruber syndrome (Q61.9)
  • Q03 Congenital hydrocephalus Incl.: hydrocephalus in newborn Excl.: Arnold-Chiari syndrome (Q07.0) hydrocephalus: acquired (G91.-) due to congenital toxoplasmosis (P37.1) with spina bifida (Q05.0-Q05.4)
  • Q04 Other congenital malformations of brain Excl.: cyclopia (Q87.0) macrocephaly (Q75.3)
  • Q05 Spina bifida Incl.: hydromeningocele (spinal), meningocele (spinal), meningomyelocele, myelocele, myelomeningocele, rachischisis, spina bifida (aperta)(cystica), syringomyelocele Excl.: Arnold-Chiari syndrome (Q07.0), spina bifida occulta (Q76.0)
  • Q06 Other congenital malformations of spinal cord
  • Q07 Other congenital malformations of nervous system Excl.: familial dysautonomia [Riley-Day] (G90.1), neurofibromatosis (nonmalignant) (Q85.0)


Links: Q00-Q07 Detailed | Neural System - Abnormalities

Congenital malformations of eye, ear, face and neck (Q10-Q18)

Links: Q10-Q18 Detailed | Head Abnormalities | Hearing Abnormalities | Vision Abnormalities | Smell Abnormalities

Excl.: cleft lip and cleft palate (Q35-Q37) congenital malformation of: cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4) larynx (Q31.-) lip NEC (Q38.0) nose (Q30.-) parathyroid gland (Q89.2) thyroid gland (Q89.2)

  • Q10 Congenital malformations of eyelid, lacrimal apparatus and orbit Excl.: cryptophthalmos: NOS (Q11.2) syndrome (Q87.0)
  • Q11 Anophthalmos, microphthalmos and macrophthalmos
  • Q12 Congenital lens malformations
  • Q13 Congenital malformations of anterior segment of eye
  • Q14 Congenital malformations of posterior segment of eye
  • Q15 Other congenital malformations of eye Excl.: congenital nystagmus (H55) ocular albinism (E70.3) retinitis pigmentosa (H35.5)
  • Q16 Congenital malformations of ear causing impairment of hearing Excl.: congenital deafness (H90.-)
  • Q17 Other congenital malformations of ear Excl.: preauricular sinus (Q18.1)
  • Q18 Other congenital malformations of face and neck Excl.: cleft lip and cleft palate (Q35-Q37) conditions classified to


Links: Q10-Q18 Detailed | Head Abnormalities | Hearing Abnormalities | Vision Abnormalities | Smell Abnormalities

Congenital malformations of the circulatory system (Q20-Q28)

Links: Q20-Q28 Detailed | Cardiovascular System - Abnormalities
  • Q20 Congenital malformations of cardiac chambers and connections Excl.: dextrocardia with situs inversus (Q89.3) mirror-image atrial arrangement with situs inversus (Q89.3)
  • Q21 Congenital malformations of cardiac septa Excl.: acquired cardiac septal defect (I51.0)
  • Q22 Congenital malformations of pulmonary and tricuspid valves
  • Q23 Congenital malformations of aortic and mitral valves
  • Q24 Other congenital malformations of heart Excl.: endocardial fibroelastosis (I42.4)
  • Q25 Congenital malformations of great arteries
  • Q26 Congenital malformations of great veins
  • Q27 Other congenital malformations of peripheral vascular system Excl.: anomalies of: cerebral and precerebral vessels (Q28.0-Q28.3) coronary vessels (Q24.5) pulmonary artery (Q25.5-Q25.7) congenital retinal aneurysm (Q14.1) haemangioma and lymphangioma (D18.-)
  • Q28 Other congenital malformations of circulatory system Excl.: congenital aneurysm: NOS (Q27.8) coronary (Q24.5) peripheral (Q27.8) pulmonary (Q25.7) retinal (Q14.1) ruptured: cerebral arteriovenous malformation (I60.8) malformation of precerebral vessels (I72.-)


ICD-11 Structural developmental anomalies of the circulatory system (draft) 
ICD-11 Beta Draft - NOT FINAL, updated on a daily basis, It is not approved by WHO, NOT TO BE USED for CODING except for agreed FIELD TRIALS.

20 Developmental Anomalies - Structural Developmental Anomalies

Beta coding and tree structure for "structural developmental anomalies" within this section are shown in the table below.

Structural developmental anomalies of the circulatory system  
  • Structural developmental anomaly of heart and great vessels
    • LB00 Congenital heart or great vessel related acquired abnormality
    • LB01 Congenital anomaly of atrioventricular or ventriculo-arterial connections
      • LB01.1 Transposition of the great arteries
      • LB01.2 Double outlet right ventricle
      • LB01.3 Double outlet left ventricle
      • LB01.4 Common arterial trunk
      • LB01.Y Other specified congenital anomaly of atrioventricular or ventriculo-arterial connections
      • LB01.Z Congenital anomaly of atrioventricular or ventriculo-arterial connections, unspecified
    • LB02 Congenital anomaly of the mediastinal veins Congenital anomaly of atria or atrial septum
    • LB20 Congenital anomaly of atrioventricular valves or septum
    • LB21 Congenital anomaly of ventricles and ventricular septum
      • LB21.1 Congenital right ventricular outflow tract obstruction  
      • LB21.2 Double-chambered right ventricle  
      • LB21.3 Tetralogy of Fallot
      • LB21.4 Congenital left ventricular outflow tract obstruction  
      • LB21.5 Congenital ventricular septal defects 
      • LB21.Y Other specified congenital anomaly of ventricles and ventricular septum
      • LB21.Z Congenital anomaly of ventricles and ventricular septum, unspecified  
    • LB22 Functionally univentricular heart
    • LB23 Congenital anomaly of ventriculo-arterial valves and adjacent regions
    • LB24 Congenital anomaly of great arteries including arterial duct
      • LB.1 Congenital aorto-pulmonary window
      • LB.2 Congenital anomaly of pulmonary arterial tree
      • LB.3 Congenital anomaly of aorta and its branches
      • LB.4 Tracheo-oesophageal compressive syndrome
      • LB.5 Patent arterial duct
      • LB.Y Other specified congenital anomaly of great arteries including arterial duct
      • LB.Z Congenital anomaly of great arteries including arterial duct, unspecified
    • LB25 Anomalous position-orientation of heart
    • LB26 Total mirror imagery
    • LB27 Left isomerism
    • LB28 Congenital anomaly of coronary arteries
    • LB29 Structural developmental anomalies of the pericardium
    • LB2Y Other specified structural developmental anomaly of heart and great vessels
    • LB2Z Structural developmental anomaly of heart and great vessels, unspecified
  • LB30 Structural developmental anomalies of the peripheral vascular system
    • LB30.1 Capillary malformations
    • LB30.2 Lymphatic malformations
      • LB30.21 Macrocystic lymphatic malformation
      • LB30.22 Microcystic lymphatic malformation
      • LB30.23 Cystic hygroma in fetus
      • BD23.1 Primary lymphoedema
          • EK91 Yellow nail syndrome
          • LC5F.26 Noonan syndrome
      • LB30.2Y Other specified lymphatic malformations
      • LB30.2Z Lymphatic malformations, unspecified
    • LB30.3 Peripheral venous malformations
    • LB30.4 Peripheral arteriovenous malformations
    • LB30.5 Peripheral arterial malformations
    • LB30.6 Pulmonary arteriovenous fistula
    • LB30.Y Other specified structural developmental anomalies of the peripheral vascular system
    • LB30.Z Structural developmental anomalies of the peripheral vascular system, unspecified
  • LB3Y Other specified structural developmental anomalies of the circulatory system
  • LB3Z Structural developmental anomalies of the circulatory system, unspecified
CD-11 Beta Draft - NOT FINAL, updated on a daily basis, It is not approved by WHO, NOT TO BE USED for CODING except for agreed FIELD TRIALS.


See also International Classification of Diseases | Abnormalities

Links: ICD10 Q20-Q28 Detailed | Cardiovascular System - Abnormalities

Congenital malformations of the respiratory system (Q30-Q34)

Links: Q30-Q34 Detailed | Respiratory Abnormalities
  • Q30 Congenital malformations of nose Excl.: congenital deviation of nasal septum (Q67.4)
  • Q31 Congenital malformations of larynx Excl.: congenital (laryngeal) stridor NOS (P28.8)
  • Q32 Congenital malformations of trachea and bronchus Excl.: congenital bronchiectasis (Q33.4)
  • Q33 Congenital malformations of lung
  • Q34 Other congenital malformations of respiratory system


Links: Q30-Q34 Detailed | Respiratory Abnormalities

Cleft lip and cleft palate (Q35-Q37)

Links: Q35-Q37 Detailed | Cleft lip and cleft palate

Use additional code (Q30.2), if desired, to identify associated malformations of the nose. Excl.: Robin's syndrome (Q87.0)

  • Q35 Cleft palate Incl.: fissure of palate palatoschisis Excl.: cleft palate with cleft lip (Q37.-)
  • Q36 Cleft lip Incl.: cheiloschisis congenital fissure of lip harelip labium leporinum Excl.: cleft lip with cleft palate (Q37.-)
  • Q37.0 Cleft hard palate with bilateral cleft lip


Links: Q35-Q37 Detailed | Cleft lip and cleft palate

Other congenital malformations of the digestive system (Q38-Q45)

  • Q38 Other congenital malformations of tongue, mouth and pharynx Excl.: macrostomia (Q18.4) microstomia (Q18.5)
  • Q39 Congenital malformations of oesophagus
  • Q40 Other congenital malformations of upper alimentary tract
  • Q41 Congenital absence, atresia and stenosis of small intestine Incl.: congenital obstruction, occlusion and stricture of small intestine or intestine NOS Excl.: meconium ileus (E84.1)
  • Q42 Congenital absence, atresia and stenosis of large intestine Incl.: congenital obstruction, occlusion and stricture of large intestine
  • Q43 Other congenital malformations of intestine
  • Q44 Congenital malformations of gallbladder, bile ducts and liver
  • Q45 Other congenital malformations of digestive system Excl.: congenital: diaphragmatic hernia (Q79.0) hiatus hernia (Q40.1)


Links: Q38-Q45 Detailed | Gastrointestinal Abnormalities

Congenital malformations of genital organs (Q50-Q56)

Links: Q50-Q56 Detailed | Genital Abnormalities

Excl.: androgen resistance syndrome (E34.5) syndromes associated with anomalies in the number and form of chromosomes (90-99) testicular feminization syndrome (E34.5)

  • Q50 Congenital malformations of ovaries, fallopian tubes and broad ligaments
  • Q51 Congenital malformations of uterus and cervix
  • Q52 Other congenital malformations of female genitalia
  • Q53 Undescended testicle
  • Q54 Hypospadias Excl.: epispadias (64.0)
  • Q55 Other congenital malformations of male genital organs Excl.: congenital hydrocele (P83.5) hypospadias (54.-)
  • Q56 Indeterminate sex and pseudohermaphroditism Excl.: pseudohermaphroditism: female, with adrenocortical disorder (E25.-) male, with androgen resistance (E34.5) with specified chromosomal anomaly (96-99)


Links: Q50-Q56 Detailed | Genital Abnormalities

Congenital malformations of the urinary system (Q60-Q64)

Links: Q60-Q64 Detailed | Renal Abnormalities | Renal Development
  • Q60 Renal agenesis and other reduction defects of kidney Incl.: atrophy of kidney: congenital infantile congenital absence of kidney
  • Q61 Cystic kidney disease Excl.: acquired cyst of kidney (N28.1) Potter's syndrome (60.6)
  • Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter
  • Q63 Other congenital malformations of kidney Excl.: congenital nephrotic syndrome (N04.-)
  • Q64 Other congenital malformations of urinary system


Links: Q60-Q64 Detailed | Renal Abnormalities | Renal Development

Congenital malformations and deformations of the musculoskeletal system

Links: Q65-Q79 Detailed | Musculoskeletal Abnormalities | Limb Abnormalities
  • Q65 Congenital deformities of hip Excl.: clicking hip (R29.4)
  • Q66 Congenital deformities of feet Excl.: reduction defects of feet (Q72.-) valgus deformities (acquired) (M21.0) varus deformities (acquired) (M21.1)
  • Q67 Congenital musculoskeletal deformities of head, face, spine and chest Excl.: congenital malformation syndromes classified to Q87.- Potter's syndrome (Q60.6)
  • Q68 Other congenital musculoskeletal deformities Excl.: reduction defects of limb(s) (Q71-Q73)
  • Q69 Polydactyly
  • Q70 Syndactyly
  • Q71 Reduction defects of upper limb
  • Q72 Reduction defects of lower limb
  • Q73 Reduction defects of unspecified limb
  • Q74 Other congenital malformations of limb(s) Excl.: polydactyly (Q69.-) reduction defect of limb (Q71-Q73) syndactyly (Q70.-)
  • Q75 Other congenital malformations of skull and face bones Excl.: congenital malformation of face NOS (Q18.-) congenital malformation syndromes classified to Q87.- dentofacial anomalies [including malocclusion] (K07.-) musculoskeletal deformities of head and face (Q67.0-Q67.4) skull defects associated with congenital anomalies of brain such as: anencephaly (Q00.0) encephalocele (Q01.-) hydrocephalus (Q03.-) microcephaly (Q02)
  • Q76 Congenital malformations of spine and bony thorax Excl.: congenital musculoskeletal deformities of spine and chest (Q67.5-Q67.8)
  • Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine Excl.: mucopolysaccharidosis (E76.0-E76.3)
  • Q78 Other osteochondrodysplasias
  • Q79 Congenital malformations of the musculoskeletal system, not elsewhere classified Excl.: congenital (sternomastoid) torticollis (Q68.0)


Links: Q65-Q79 Detailed | Musculoskeletal Abnormalities | Limb Abnormalities

Other congenital malformations (Q80-Q89)

Links: Q80-Q89 Detailed | Integumentary Abnormalities
  • Q80 Congenital ichthyosis
  • Q81 Epidermolysis bullosa
  • Q83 Congenital malformations of breast
  • Q84 Other congenital malformations of integument
  • Q85 Phakomatoses, not elsewhere classified
  • Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
  • Q87 Other specified congenital malformation syndromes affecting multiple systems
  • Q89 Other congenital malformations, not elsewhere classified


Links: Q80-Q89 Detailed | Integumentary Abnormalities

Chromosomal abnormalities, not elsewhere classified (Q90-Q99)

Links: Q90-Q99 Detailed | Genetic Abnormalities | Trisomy 21 | Trisomy 18 | Trisomy 13 | Trisomy X | Philadelphia chromosome | Disorders of Sex Development
  • Q90 Down's syndrome
  • Q91 Edwards' syndrome and Patau's syndrome
  • Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified Incl.: unbalanced translocations and insertions Excl.: trisomies of chromosomes 13, 18, 21 (Q90-Q91)
  • Q93 Monosomies and deletions from the autosomes, not elsewhere classified
  • Q95 Balanced rearrangements and structural markers, not elsewhere classified Incl.: Robertsonian and balanced reciprocal translocations and insertions
  • Q96 Turner's syndrome Excl.: Noonan's syndrome (Q87.1)
  • Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified Excl.: Turner's syndrome (Q96.-)
  • Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified
  • Q99 Other chromosome abnormalities, not elsewhere classified


Links: Q90-Q99 Detailed | Genetic Abnormalities | Trisomy 21 | Trisomy 18 | Trisomy 13 | Trisomy X | Philadelphia chromosome | Disorders of Sex Development

ICD-10 Chapter XVI Certain conditions originating in the perinatal period (P00-P96)

Includes conditions that have their origin in the perinatal period even though death or morbidity occurs later.

Excludes congenital malformations, deformations and chromosomal abnormalities (Q00-Q99); endocrine, nutritional and metabolic diseases (E00-E90); injury, poisoning and certain other consequences of external causes (S00-T98); neoplasms (C00-D48); tetanus neonatorum (A33)



Links: Chapter XVI Perinatal Period | Neonatal Development | Neonatal Diagnosis

ICD-10 Chapter XV Pregnancy, childbirth and the puerperium (O00-O99)

The codes included in this chapter are to be used for conditions related to or aggravated by the pregnancy, childbirth or by the puerperium (maternal causes or obstetric causes)

Excludes Certain diseases or injuries complicating pregnancy, childbirth and the puerperium classified elsewhere: external causes (for mortality) (V, W, X, Y); injury, poisoning and certain other consequences of external cause (S00-T88.1, , T88.6-T98); mental and behavioural disorders associated with the puerperium (F53.-); obstetrical tetanus (A34); postpartum necrosis of pituitary gland (E23.0); puerperal osteomalacia (M83.0); supervision of high-risk pregnancy (Z35.-); supervision of normal pregnancy (Z34.-).



Links: ICD-10 Chapter XV Pregnancy Childbirth | birth