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HomeICD10Chapter17

Posts in category: ICD10Chapter17

Q83.1 Accessory breast Notes: Supernumerary breast

by dr.kijakarn junda MD. first class hon. , FRCP(t) ICD10_2023ICD10Chapter17

Accessory breast Notes: Supernumerary breast

Q85.0 Neurofibromatosis (nonmalignant) Notes: Von Recklinghausen disease ; Acoustic neurofibromatosis

by dr.kijakarn junda MD. first class hon. , FRCP(t) ICD10_2023ICD10Chapter17

Neurofibromatosis (nonmalignant) Notes: Von Recklinghausen disease ; Acoustic neurofibromatosis

Q86.2 Dysmorphism due to warfarin

by dr.kijakarn junda MD. first class hon. , FRCP(t) ICD10_2023ICD10Chapter17

Dysmorphism due to warfarin

Q87.5 Other congenital malformation syndromes with other skeletal changes

by dr.kijakarn junda MD. first class hon. , FRCP(t) ICD10_2023ICD10Chapter17

Other congenital malformation syndromes with other skeletal changes

Q90 Down syndrome Notes: Trisomy 21 NOS ; code(s) to identify any associated physical conditions and degree of intellectual …

by dr.kijakarn junda MD. first class hon. , FRCP(t) ICD10_2023ICD10Chapter17

Down syndrome Notes: Trisomy 21 NOS ; code(s) to identify any associated physical conditions and degree of intellectual disabilities (F70-F79)

Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)

by dr.kijakarn junda MD. first class hon. , FRCP(t) ICD10_2023ICD10Chapter17

Whole chromosome trisomy, mosaicism (mitotic nondisjunction)

Q93.51 Angelman syndrome

by dr.kijakarn junda MD. first class hon. , FRCP(t) ICD10_2023ICD10Chapter17

Angelman syndrome

Q77.0 Achondrogenesis Notes: Hypochondrogenesis

by dr.kijakarn junda MD. first class hon. , FRCP(t) ICD10_2023ICD10Chapter17

Achondrogenesis Notes: Hypochondrogenesis

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ICD10Chapter17

  • Q98.0 Klinefelter syndrome karyotype 47, XXY
    Klinefelter syndrome karyotype 47, XXY Share
  • Q98 Other sex chromosome abnormalities, male pheno…
    Other sex chromosome abnormalities, male phenotype, not elsewhere classified Share
  • Q97.9 Sex chromosome abnormality, female phenotype…
    Sex chromosome abnormality, female phenotype, unspecified Share
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