Talk:International Classification of Diseases: Difference between revisions
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deformity | deformity | ||
NOS of urinary system | 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 |
Revision as of 20:08, 10 July 2012
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