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Intersex Genital Mutilations in ICD-10 Zwischengeschlecht.Org / Stopigm.Org 2014 (V2.1)

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Intersex Genital Mutilations in ICD-10 Zwischengeschlecht.Org / Stopigm.Org 2014 (V2.1) Intersex Genital Mutilations in ICD-10 Zwischengeschlecht.org / StopIGM.org 2014 (v2.1) ICD-10 Codes and Descriptions: http://apps.who.int/classifications/icd10/browse/2010/en 1. Reference: 17 Most Common IGM Procedures (a–q) Source: 2014 CRC NGO Report, Supplement 2 “Most Common Forms of IGMs”, p. 63–76: http://intersex.shadowreport.org/public/2014-CRC-Swiss-NGO-Zwischengeschlecht-Intersex-IGM_v2.pdf a) Clitoris Amputation/“Reduction”/“Recession” 63 b) Hypospadias “Repair” 65 c) Castrations / “Gonadectomies” / Hysterectomies / (Secondary) Sterilisation 67 d) “Vaginoplasty”, Construction of Artificial “Neo Vagina” 69 e) Forced Vaginal Dilation 69 f) Forced Mastectomy 70 g) Surgical Transfixation of Undescended Testes 70 h) Imposition of Hormones 70 i) Misinformation and Directive Counselling for Parents 70 j) Taking Advantage of the Powerlessness and Vulnerability of Intersex Infants 72 k) Systematic Lies and Imposition of “Code of Silence” on Children 72 l) Forced Excessive Genital Exams, Medical Display and (Genital) Photography 73 m) Human Experimentation on Intersex Children 74 n) Denial of Needed Health Care 75 o) Prenatal “Therapy” 75 p) Selective Abortion, Selective Late Term Abortion 76 q) Preimplantation Genetic Diagnosis (PGD) to Eliminate Intersex Fetuses 76 2. IGMs: List of Relevant ICD-10 Codes Chapter IV. Endocrine, nutritional and metabolic diseases Disorders of other endocrine glands (E20—E35) E23.0 Hypopituitarism Fertile eunuch syndrome Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of: gonadotropin growth hormone pituitary hormone Kallmann syndrome Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary: cachexia insufficiency NOS short stature Sheehan syndrome Simmonds disease 1 E25 Adrenogenital disorders a, b, c, d, e, f, h, i, j, k, l, m, n, o, p, q E25.0 Congenital adrenogenital disorders associated with enzyme deficiency Congenital adrenal hyperplasia 21-Hydroxylase deficiency Salt-losing congenital adrenal hyperplasia E25.8 Other adrenogenital disorders Idiopathic adrenogenital disorder E25.9 Adrenogenital disorder, unspecified Adrenogenital syndrome NOS E28. Androgen excess Hypersecretion of ovarian androgens E29. Testicular dysfunction E29.0 Testicular hyperfunction Hypersecretion of testicular hormones E29.1 Testicular hypofunction a, b, c, d, e, g, h, i, j, k, l, m, n, o, p, q 5-Alpha-reductase deficiency (with male pseudohermaphroditism) Defective biosynthesis of testicular androgen NOS Testicular hypogonadism NOS Use additional external cause code (Chapter XX), if desired, to identify drug, if drug- induced. E29.8 Other testicular dysfunction E29.9 Testicular dysfunction, unspecified E30 Disorders of puberty, not elsewhere classified E30.0 Delayed puberty Constitutional delayed puberty Delayed sexual development E34 Other endocrine disorders E34.5 Androgen resistance syndrome a, b, c, d, e, f, g, h, i, j, k, l, m, n, o, p, q Male pseudohermaphroditism with androgen resistance Peripheral hormonal receptor disorder Reifenstein syndrome Testicular feminization (syndrome) --> N46, N48, N50.0 Chapter XVII Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) Congenital malformations of genital organs (Q50-Q56) Q50 Congenital malformations of ovaries, fallopian tubes and broad ligaments Q50.0 Congenital absence of ovary Q50.3 Other congenital malformations of ovary Accessory ovary Congenital malformation of ovary NOS Congenital malformation of fallopian tube or broad ligament NOS Q51 Congenital malformations of uterus and cervix 2 Q51.0Agenesis and aplasia of uterus Congenital absence of uterus Q51.5 Agenesis and aplasia of cervix Congenital absence of cervix Q51.6 Embryonic cyst of cervix Q51.7 Congenital fistulae between uterus and digestive and urinary tracts Q51.8 Other congenital malformations of uterus and cervix Hypoplasia of uterus and cervix Q51.9 Congenital malformation of uterus and cervix, unspecified Q52 Other congenital malformations of female genitalia Q52.0 Congenital absence of vagina d, e, i, j, k, l, m, n, o Q52.1 Doubling of vagina Q52.4 Other congenital malformations of vagina Congenital malformation of vagina NOS Q52.5 Fusion of labia Q52.6 Congenital malformation of clitoris Q52.7 Other congenital malformations of vulva Q52.8 Other specified congenital malformations of female genitalia Q52.9 Congenital malformation of female genitalia, unspecified Q53Undescended testicle g, h, i, j, k, l, m, n, o Q53.0 Ectopic testis Unilateral or bilateral ectopic testes Q53.1 Undescended testicle, unilateral Q53.2 Undescended testicle, bilateral Q53.9 Undescended testicle, unspecified Cryptorchism NOS Q54Hypospadias b, i, j, k, l, m, n, o Q54.0 Hypospadias, balanic Hypospadias: coronal glandular Q54.1 Hypospadias, penile Q54.2 Hypospadias, penoscrotal Q54.3 Hypospadias, perineal Q54.4 Congenital chordee Q54.8 Other hypospadias Q54.9 Hypospadias, unspecified Q55 Other congenital malformations of male genital organs Q55.0 Absence and aplasia of testis Monorchism Q55.1 Hypoplasia of testis and scrotum Fusion of testes Q55.2 Other congenital malformations of testis and scrotum Congenital malformation of testis or scrotum NOS Polyorchism 3 Retractile testis g, h, i, j, k, l, m, n, o Testis migrans g, h, i, j, k, l, m, n, o Q55.3 Atresia of vas deferens Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate Q55.5 Congenital absence and aplasia of penis Q55.6 Other congenital malformations of penis Congenital malformation of penis NOS Curvature of penis (lateral) Hypoplasia of penis Q55.8 Other specified congenital malformations of male genital organs Q55.9 Congenital malformation of male genital organ, unspecified Q56 Indeterminate sex and pseudohermaphroditism a, b, c, d, e, f, g, h, i, j, k, l, m, n, o Q56.0 Hermaphroditism, not elsewhere classified Ovotestis Q56.1 Male pseudohermaphroditism, not elsewhere classified Male pseudohermaphroditism NOS Q56.2 Female pseudohermaphroditism, not elsewhere classified Female pseudohermaphroditism NOS Q56.3 Pseudohermaphroditism, unspecified Q56.4 Indeterminate sex, unspecified Ambiguous genitalia Other congenital malformations (Q80-89) Congenital malformations of breast Q83.0 Congenital absence of breast with absent nipple Q83.1 Accessory breast Supernumerary breast Q83.2 Absent nipple Q83.3 Accessory nipple Supernumerary nipple Q83.8 Other congenital malformations of breast Hypoplasia of breast Q83.9 Congenital malformation of breast, unspecified Other congenital malformations, not elsewhere classified (Q90-99) Q96Turner syndrome p, q Q96.0 Karyotype 45,X Q96.1 Karyotype 46,X iso (Xq) Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq) Q96.3 Mosaicism, 45,X/46,XX or XY Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome Q96.8 Other variants of Turner syndrome Q96.9 Turner syndrome, unspecified Q97Other sex chromosome abnormalities, female phenotype, not elsewhere classified Q97.0 Karyotype 47,XXX Q97.1 Female with more than three X chromosomes 4 Q97.2 Mosaicism, lines with various numbers of X chromosomes Q97.3 Female with 46,XY karyotype Q97.8 Other specified sex chromosome abnormalities, female phenotype Q97.9 Sex chromosome abnormality, female phenotype, unspecified Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified f, h, p, q Q98.0 Klinefelter syndrome karyotype 47,XXY Q98.1 Klinefelter syndrome, male with more than two X chromosomes Q98.2 Klinefelter syndrome, male with 46,XX karyotype Q98.3 Other male with 46,XX karyotype Q98.4 Klinefelter syndrome, unspecified Q98.5 Karyotype 47,XYY Q98.6 Male with structurally abnormal sex chromosome Q98.7 Male with sex chromosome mosaicism Q98.8 Other specified sex chromosome abnormalities, male phenotype Q98.9 Sex chromosome abnormality, male phenotype, unspecified Q99 Other chromosome abnormalities, not elsewhere classified a, b, c, d, e, f, g, h, i, j, k, l, m, n, o, p, q Q99.0 Chimera 46,XX/46,XY Chimera 46,XX/46,XY true hermaphrodite Q99.1 46,XX true hermaphrodite 46,XX with streak gonads 46,XY with streak gonads Pure gonadal dysgenesis Q99.2 Fragile X chromosome Fragile X syndrome 5.
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