Talk:International Classification of Diseases

From Embryology

Congenital malformations of the urinary system (Q60-Q64)

  • Q60 Renal agenesis and other reduction defects of kidney Incl.: atrophy of kidney: congenital infantile congenital absence of kidney
    • Q60.0 Renal agenesis, unilateral
    • Q60.1 Renal agenesis, bilateral
    • Q60.2 Renal agenesis, unspecified
    • Q60.3 Renal hypoplasia, unilateral
    • Q60.4 Renal hypoplasia, bilateral
    • Q60.5 Renal hypoplasia, unspecified
    • Q60.6 Potter's syndrome
  • Q61 Cystic kidney disease Excl.: acquired cyst of kidney (N28.1) Potter's syndrome (Q60.6)
    • Q61.0 Congenital single renal cyst Cyst of kidney (congenital)(single)
    • Q61.1 Polycystic kidney, autosomal recessive Polycystic kidney, infantile type
    • Q61.2 Polycystic kidney, autosomal dominant Polycystic kidney, adult type
    • Q61.3 Polycystic kidney, unspecified
    • Q61.4 Renal dysplasia Multicystic: dyplastic kidney kidney (developmental) kidney disease Renal dysplasia Excl.:polycystic kidney disease (Q61.1-Q61.3)
    • Q61.5 Medullary cystic kidney Sponge kidney NOS
    • Q61.8 Other cystic kidney diseases Fibrocystic: kidney Renal degeneration or disease
    • Q61.9 Cystic kidney disease, unspecified Meckel-Gruber syndrome
  • Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter
    • Q62.0 Congenital hydronephrosis
    • Q62.1 Atresia and stenosis of ureter Congenital occlusion of: ureter ureteropelvic junction ureterovesical orifice Impervious ureter
    • Q62.2 Congenital megaloureter Congenital dilatation of ureter
    • Q62.3 Other obstructive defects of renal pelvis and ureter Congenital ureterocele
    • Q62.4 Agenesis of ureter Absent ureter
    • Q62.5 Duplication of ureter Accessory Double ureter
    • Q62.6 Malposition of ureter Deviation, Displacement, Ectopic Implantation, anomalous (of) ureter or ureteric orifice
    • Q62.7 Congenital vesico-uretero-renal reflux
    • Q62.8 Other congenital malformations of ureter Anomaly of ureter NOS
  • Q63 Other congenital malformations of kidney Excl.: congenital nephrotic syndrome (N04.-)
    • Q63.0 Accessory kidney
    • Q63.1 Lobulated, fused and horseshoe kidney
    • Q63.2 Ectopic kidney Congenital displaced kidney Malrotation of kidney
    • Q63.3 Hyperplastic and giant kidney
    • Q63.8 Other specified congenital malformations of kidney Congenital renal calculi
    • Q63.9 Congenital malformation of kidney, unspecified
  • Q64 Other congenital malformations of urinary system
    • Q64.0 Epispadias Excl.: hypospadias (Q54.-)
    • Q64.1 Exstrophy of urinary bladder

Ectopia vesicae Extroversion of bladder

    • Q64.2 Congenital posterior urethral valves
    • Q64.3 Other atresia and stenosis of urethra and bladder neck

Congenital: bladder neck obstruction stricture of: urethra urinary meatus vesicourethral orifice Impervious urethra

    • Q64.4 Malformation of urachus

Cyst of urachus Patent urachus Prolapse of urachus

    • Q64.5 Congenital absence of bladder and urethra
    • Q64.6 Congenital diverticulum of bladder
    • Q64.7 Other congenital malformations of bladder and urethra

Accessory: bladder urethra Congenital: hernia of bladder malformation of bladder or urethra NOS prolapse of: bladder (mucosa) urethra urinary meatus urethrorectal fistula Double: urethra urinary meatus

    • Q64.8 Other specified congenital malformations of urinary system
    • Q64.9 Congenital malformation of urinary system, unspecified

Congenital: anomaly deformity NOS of urinary system


Other congenital malformations (Q80-Q89)

  • Q80 Congenital ichthyosis Excl.: Refsum's disease (G60.1)
    • Q80.0 Ichthyosis vulgaris
    • Q80.1 X-linked ichthyosis
    • Q80.2 Lamellar ichthyosis Collodion baby
    • Q80.3 Congenital bullous ichthyosiform erythroderma
    • Q80.4 Harlequin fetus
    • Q80.8 Other congenital ichthyosis
    • Q80.9 Congenital ichthyosis, unspecified
  • Q81 Epidermolysis bullosa
    • Q81.0 Epidermolysis bullosa simplex Excl.: Cockayne's syndrome (Q87.1)
    • Q81.1

Epidermolysis bullosa letalis Herlitz' syndrome

    • Q81.2

Epidermolysis bullosa dystrophica

    • Q81.8

Other epidermolysis bullosa

    • Q81.9

Epidermolysis bullosa, unspecified

  • Q82 Other congenital malformations of skin

Excl.: acrodermatitis enteropathica (E83.2) congenital erythropoietic porphyria (E80.0) pilonidal cyst or sinus (L05.-) Sturge-Weber(-Dimitri) syndrome (** Q85.8)

    • Q82.0

Hereditary lymphoedema

    • Q82.1

Xeroderma pigmentosum

    • Q82.2

Mastocytosis Urticaria pigmentosa Excl.: malignant mastocytosis (C96.2)

    • Q82.3

Incontinentia pigmenti

    • Q82.4

Ectodermal dysplasia (anhidrotic) Excl.: Ellis-van Creveld syndrome (** Q77.6)

    • Q82.5

Congenital non-neoplastic naevus Birthmark NOS Naevus: flammeus portwine sanguineous strawberry vascular NOS verrucous Excl.: café au lait spots (L81.3) lentigo (L81.4) naevus: NOS (D22.-) araneus (I78.1) melanocytic (D22.-) pigmented (D22.-) spider (I78.1) stellar (I78.1)

    • Q82.8

Other specified congenital malformations of skin Abnormal palmar creases Accessory skin tags Benign familial pemphigus [Hailey-Hailey] Cutis laxa (hyperelastica) Dermatoglyphic anomalies Inherited keratosis palmaris et plantaris Keratosis follicularis [Darier-White] Excl.: Ehlers-Danlos syndrome (** Q79.6)

    • Q82.9 Congenital malformation of skin, unspecified
  • Q83 Congenital malformations of breast

Excl.: absence of pectoral muscle (** Q79.8)

    • 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

  • Q84 Other congenital malformations of integument
    • Q84.0

Congenital alopecia Congenital atrichosis

    • Q84.1

Congenital morphological disturbances of hair, not elsewhere classified Beaded hair Monilethrix Pili annulati Excl.: Menkes' kinky hair syndrome (E83.0)

    • Q84.2

Other congenital malformations of hair Congenital: hypertrichosis malformation of hair NOS Persistent lanugo

    • Q84.3

Anonychia Excl.: nail patella syndrome (** Q87.2)

    • Q84.4

Congenital leukonychia

  • Q84.5 Enlarged and hypertrophic nails

Congenital onychauxis Pachyonychia

    • Q84.6

Other congenital malformations of nails Congenital: clubnail koilonychia malformation of nail NOS

    • Q84.8

Other specified congenital malformations of integument Aplasia cutis congenita

    • Q84.9

Congenital malformation of integument, unspecified Congenital: anomaly NOS deformity NOS of integument NOS

  • Q85 Phakomatoses, not elsewhere classified

Excl.: ataxia telangiectasia [Louis-Bar] (G11.3) familial dysautonomia [Riley-Day] (G90.1)

    • Q85.0

Neurofibromatosis (nonmalignant) Von Recklinghausen's disease

    • Q85.1

Tuberous sclerosis Bourneville's disease Epiloia

    • Q85.8

Other phakomatoses, not elsewhere classified Syndrome: Peutz-Jeghers Sturge-Weber(-Dimitri) von Hippel-Lindau Excl.: Meckel-Gruber syndrome (** Q61.9)

    • Q85.9

Phakomatosis, unspecified Hamartosis NOS

  • Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified

Excl.: iodine-deficiency-related hypothyroidism (E00-E02) nonteratogenic effects of substances transmitted via placenta or breast milk (P04.-)

    • Q86.0

Fetal alcohol syndrome (dysmorphic)

    • Q86.1

Fetal hydantoin syndrome Meadow's syndrome

    • Q86.2

Dysmorphism due to warfarin

    • Q86.8

Other congenital malformation syndromes due to known exogenous causes

  • Q87 Other specified congenital malformation syndromes affecting multiple systems
    • Q87.0

Congenital malformation syndromes predominantly affecting facial appearance Acrocephalopolysyndactyly Acrocephalosyndactyly [Apert] Cryptophthalmos syndrome Cyclopia Syndrome: Goldenhar Moebius oro-facial-digital Robin Whistling face

    • Q87.1

Congenital malformation syndromes predominantly associated with short stature Syndrome: Aarskog Cockayne De Lange Dubowitz Noonan Prader-Willi Robinow-Silverman-Smith Russell-Silver Seckel Smith-Lemli-Opitz Excl.: Ellis-van Creveld syndrome (** Q77.6)

    • Q87.2

Congenital malformation syndromes predominantly involving limbs Syndrome: Holt-Oram Klippel-Trénaunay-Weber nail patella Rubinstein-Taybi sirenomelia thrombocytopenia with absent radius [TAR] VATER

    • Q87.3

Congenital malformation syndromes involving early overgrowth Syndrome: Beckwith-Wiedemann Sotos Weaver

    • Q87.4

Marfan's syndrome

    • Q87.5

Other congenital malformation syndromes with other skeletal changes

    • Q87.8

Other specified congenital malformation syndromes, not elsewhere classified Syndrome: Alport Laurence-Moon(-Bardet)-Biedl Zellweger

  • Q89 Other congenital malformations, not elsewhere classified
    • Q89.0

Congenital malformations of spleen Asplenia (congenital) Congenital splenomegaly Excl.: isomerism of atrial appendages (with asplenia or polysplenia) (** Q20.6)

    • Q89.1

Congenital malformations of adrenal gland Excl.: congenital adrenal hyperplasia (E25.0)

    • Q89.2

Congenital malformations of other endocrine glands Congenital malformation of parathyroid or thyroid gland Persistent thyroglossal duct Thyroglossal cyst

    • Q89.3

Situs inversus Dextrocardia with situs inversus Mirror-image atrial arrangement with situs inversus Situs inversus or transversus: abdominalis thoracis Transposition of viscera: abdominal thoracic Excl.: dextrocardia NOS (** Q24.0) laevocardia (** Q24.1)

    • Q89.4

Conjoined twins Craniopagus Dicephaly Double monster Pygopagus Thoracopagus

    • Q89.7

Multiple congenital malformations, not elsewhere classified Monster NOS Multiple congenital: anomalies NOS deformities NOS Excl.: congenital malformation syndromes affecting multiple systems (** Q87.-)

    • Q89.8

Other specified congenital malformations

    • Q89.9

Congenital malformation, unspecified Congenital: anomaly NOS deformity NOS

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