ICD-10 บท Q: รูปวิปริตแต่กำเนิด การแปลงรูปและโครโมโซมผิดปกติ - วิกิพีเดีย

# ICD-10 บท Q: รูปวิปริตแต่กำเนิด การแปลงรูปและโครโมโซมผิดปกติ

### จากวิกิพีเดีย สารานุกรมเสรี

## [แก้] Q00-Q89 - รูปพิการและการแปลงรูป แต่กำเนิด

### [แก้] (Q00-Q07) nervous system

- (Q00) Anencephaly and similar malformations
- (Q01) Encephalocele
- (Q02) Microcephaly
- (Q03) Congenital hydrocephalus
- (Q04) Other congenital malformations of brain
- (Q05) Spina bifida
- (Q06) Other congenital malformations of spinal cord
- (Q07) Other congenital malformations of nervous system

### [แก้] (Q10-Q18) eye, ear, face and neck

- (Q10) Congenital malformations of eyelid, lacrimal apparatus and orbit
- (Q11) Anophthalmos, microphthalmos and macrophthalmos
- (Q12) Congenital lens malformations
- (Q13) Congenital malformations of anterior segment of eye
  - (Q131) Absence of iris
    - Aniridia
- (Q14) Congenital malformations of posterior segment of eye
- (Q15) Other congenital malformations of eye
  - (Q150) Congenital glaucoma
- (Q16) Congenital malformations of ear causing impairment of hearing
- (Q17) Other congenital malformations of ear
- (Q18) Other congenital malformations of face and neck

### [แก้] (Q20-Q28) circulatory system

- (Q20) Congenital malformations of cardiac chambers and connections
  - (Q200) Common arterial trunk
    - Persistent truncus arteriosus
  - (Q201) Double outlet right ventricle
    - Taussig-Bing syndrome
  - (Q203) Discordant ventriculoarterial connection
    - Dextrotransposition of aorta
    - Transposition of great vessels (complete)
  - (Q205) Discordant atrioventricular connection
    - Corrected transposition
- (Q21) Congenital malformations of cardiac septa
  - (Q210) Ventricular septal defect
  - (Q211) Atrial septal defect
  - (Q212) Atrioventricular septal defect
  - (Q213) Tetralogy of Fallot
  - (Q218) Other congenital malformations of cardiac septa
    - Eisenmenger's syndrome

- (Q22) Congenital malformations of pulmonary and tricuspid valves
  - (Q220) Pulmonary valve atresia
  - (Q221) Congenital pulmonary valve stenosis
  - (Q222) Congenital pulmonary valve insufficiency
  - (Q223) Other congenital malformations of pulmonary valve
  - (Q224) Congenital tricuspid stenosis
    - Tricuspid atresia
  - (Q225) Ebstein's anomaly
  - (Q226) Hypoplastic right heart syndrome
  - (Q228) Other congenital malformations of tricuspid valve
  - (Q229) Congenital malformation of tricuspid valve, unspecified

- (Q23) Congenital malformations of aortic and mitral valves
  - (Q230) Congenital stenosis of aortic valve
  - (Q234) Hypoplastic left heart syndrome
- (Q24) Other congenital malformations of heart
  - (Q240) Dextrocardia
  - (Q242) Cor triatriatum
- (Q25) Congenital malformations of great arteries
  - (Q250) Patent ductus arteriosus
  - (Q251) Coarctation of aorta
  - (Q254) Other congenital malformations of aorta
    - (Q25.42) Overriding aorta
  - (Q255) Atresia of pulmonary artery
- (Q26) Congenital malformations of great veins
  - (Q262) Total anomalous pulmonary venous connection
  - (Q268) Other congenital malformations of great veins
    - Scimitar syndrome
- (Q27) Other congenital malformations of peripheral vascular system
- (Q28) Other congenital malformations of circulatory system

### [แก้] (Q30-Q34) respiratory system

- (Q30) [[Congenital malformations of nose
  - (Q300) Choanal atresia
  - (Q301) Agenesis and underdevelopment of nose
  - (Q302) Fissured, notched and cleft nose
  - (Q303) Congenital perforated nasal septum
  - (Q308) Other congenital malformations of nose
  - (Q309) Congenital malformation of nose, unspecified

- (Q31) Congenital malformations of larynx
  - (Q310) Web of larynx
  - (Q311) Congenital subglottic stenosis
  - (Q312) Laryngeal hypoplasia
  - (Q313) Laryngocele
  - (Q315) Congenital laryngomalacia
  - (Q318) Other congenital malformations of larynx
  - (Q319) Congenital malformation of larynx, unspecified

- (Q32) Congenital malformations of trachea and bronchus
  - (Q320) Congenital tracheomalacia
  - (Q321) Other congenital malformations of trachea
  - (Q322) Congenital bronchomalacia
  - (Q323) Congenital stenosis of bronchus
  - (Q324) Other congenital malformations of bronchus

- (Q33) Congenital malformations of lung
  - (Q330) Congenital cystic lung
  - (Q331) Accessory lobe of lung
  - (Q332) Sequestration of lung
  - (Q333) Agenesis of lung
  - (Q334) Congenital bronchiectasis
  - (Q335) Ectopic tissue in lung
  - (Q336) Hypoplasia and dysplasia of lung
  - (Q338) Other congenital malformations of lung
  - (Q339) Congenital malformation of lung, unspecified

- (Q34) Other congenital malformations of respiratory system
  - (Q340) Anomaly of pleura
  - (Q341) Congenital cyst of mediastinum
  - (Q348) Other specified congenital malformations of respiratory system
  - (Q349) Congenital malformation of respiratory system, unspecified

### [แก้] (Q35-Q45) digestive system

- (Q35) Cleft palate
- (Q36) Cleft lip
- (Q37) Cleft palate with cleft lip

- (Q38) Other congenital malformations of tongue, mouth and pharynx
  - (Q380) Congenital malformations of lips, not elsewhere classified
    - Van der Woude's syndrome
  - (Q387) Pharyngeal pouch
- (Q39) Congenital malformations of oesophagus
- (Q40) Other congenital malformations of upper alimentary tract
  - (Q400) Congenital hypertrophic pyloric stenosis
  - (Q401) Congenital hiatus hernia
- (Q41) Congenital absence, atresia and stenosis of small intestine
- (Q42) Congenital absence, atresia and stenosis of large intestine

- (Q43) Other congenital malformations of intestine
  - (Q430) Meckel's diverticulum
  - (Q431) Hirschsprung's disease
  - (Q432) Other congenital functional disorders of colon
  - (Q433) Congenital malformations of intestinal fixation
  - (Q434) Duplication of intestine
  - (Q435) Ectopic anus
  - (Q436) Congenital fistula of rectum and anus
  - (Q437) Persistent cloaca
  - (Q438) Other specified congenital malformations of intestine

- (Q44) Congenital malformations of gallbladder, bile ducts and liver
- (Q45) Other congenital malformations of digestive system

### [แก้] (Q50-Q56) genital organs

- (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
- (Q55) Other congenital malformations of male genital organs
- (Q56) Indeterminate sex and pseudohermaphroditism

### [แก้] (Q60-Q64) urinary system

- (Q60) Renal agenesis and other reduction defects of kidney
- (Q61) Cystic kidney disease
- (Q62) Congenital obstructive defects of renal pelvis and congenital malformations of ureter
- (Q63) Other congenital malformations of kidney
- (Q64) Other congenital malformations of urinary system

### [แก้] (Q65-Q79) musculoskeletal system

- (Q65) Congenital deformities of hip
  - (Q650) Congenital dislocation of hip, unilateral
  - (Q651) Congenital dislocation of hip, bilateral
  - (Q652) Congenital dislocation of hip, unspecified
  - (Q653) Congenital subluxation of hip, unilateral
  - (Q654) Congenital subluxation of hip, bilateral
  - (Q655) Congenital subluxation of hip, unspecified
  - (Q656) Unstable hip
  - (Q658) Other congenital deformities of hip
  - (Q659) Congenital deformity of hip, unspecified

- (Q66) Congenital deformities of feet
  - (Q660) Talipes equinovarus
  - (Q661) Talipes calcaneovarus
  - (Q662) Metatarsus varus
  - (Q663) Other congenital varus deformities of feet
  - (Q664) Talipes calcaneovalgus
  - (Q665) Congenital pes planus
  - (Q666) Other congenital valgus deformities of feet
  - (Q667) Pes cavus
  - (Q668) Other congenital deformities of feet
  - (Q669) Congenital deformity of feet, unspecified

- (Q67) Congenital musculoskeletal deformities of head, face, spine and chest
  - (Q670) Facial asymmetry
  - (Q671) Compression facies
  - (Q672) Dolichocephaly
  - (Q673) Plagiocephaly
  - (Q674) Other congenital deformities of skull, face and jaw
  - (Q675) Congenital deformity of spine
  - (Q676) Pectus excavatum
  - (Q677) Pectus carinatum
  - (Q678) Other congenital deformities of chest

- (Q68) Other congenital musculoskeletal deformities
  - (Q680) Congenital deformity of sternocleidomastoid muscle
  - (Q681) Congenital deformity of hand
  - (Q682) Congenital deformity of knee
  - (Q683) Congenital bowing of femur
  - (Q684) Congenital bowing of tibia and fibula
  - (Q685) Congenital bowing of long bones of leg, unspecified
  - (Q688) Other specified congenital musculoskeletal deformities

- (Q69) Polydactyly
  - (Q690) Accessory finger(s)
  - (Q691) Accessory thumb(s)
  - (Q692) Accessory toe(s)
  - (Q699) Polydactyly, unspecified

- (Q70) Syndactyly
  - (Q700) Fused fingers
  - (Q701) Webbed fingers
  - (Q702) Fused toes
  - (Q703) Webbed toes
  - (Q704) Polysyndactyly
  - (Q709) Syndactyly, unspecified

- (Q71) Reduction defects of upper limb
  - (Q710) Congenital complete absence of upper limb(s)
  - (Q711) Congenital absence of upper arm and forearm with hand present
  - (Q712) Congenital absence of both forearm and hand
  - (Q713) Congenital absence of hand and finger(s)
  - (Q714) Longitudinal reduction defect of radius
  - (Q715) Longitudinal reduction defect of ulna
  - (Q716) Lobster-claw hand
  - (Q718) Other reduction defects of upper limb(s)
  - (Q719) Reduction defect of upper limb, unspecified

- (Q72) Reduction defects of lower limb
  - (Q720) Congenital complete absence of lower limb(s)
  - (Q721) Congenital absence of thigh and lower leg with foot present
  - (Q722) Congenital absence of both lower leg and foot
  - (Q723) Congenital absence of foot and toe(s)
  - (Q724) Longitudinal reduction defect of femur
  - (Q725) Longitudinal reduction defect of tibia
  - (Q726) Longitudinal reduction defect of fibula
  - (Q727) Split foot
  - (Q728) Other reduction defects of lower limb(s)
  - (Q729) Reduction defect of lower limb, unspecified

- (Q73) Reduction defects of unspecified limb
  - (Q730) Congenital absence of unspecified limb(s)
  - (Q731) Phocomelia, unspecified limb(s)
  - (Q738) Other reduction defects of unspecified limb(s)

- (Q74) Other congenital malformations of limb(s)
  - (Q740) Other congenital malformations of upper limb(s), including shoulder girdle
  - (Q741) Congenital malformation of knee
  - (Q742) Other congenital malformations of lower limb(s), including pelvic girdle
  - (Q743) Arthrogryposis multiplex congenita
  - (Q748) Other specified congenital malformations of limb(s)
  - (Q749) Unspecified congenital malformation of limb(s)

- (Q75) Other congenital malformations of skull and face bones
  - (Q750) Craniosynostosis
  - (Q751) Craniofacial dysostosis
  - (Q752) Hypertelorism
  - (Q753) Macrocephaly
  - (Q754) Mandibulofacial dysostosis
  - (Q755) Oculomandibular dysostosis
  - (Q758) Other specified congenital malformations of skull and face bones
  - (Q759) Congenital malformation of skull and face bones, unspecified

- (Q76) Congenital malformations of spine and bony thorax
  - (Q760) Spina bifida occulta
  - (Q761) Klippel-Feil syndrome
  - (Q762) Congenital spondylolisthesis
  - (Q763) Congenital scoliosis due to congenital bony malformation
  - (Q764) Other congenital malformations of spine, not associated with scoliosis
  - (Q765) Cervical rib
  - (Q766) Other congenital malformations of ribs
  - (Q767) Congenital malformation of sternum
  - (Q768) Other congenital malformations of bony thorax
  - (Q769) Congenital malformation of bony thorax, unspecified

- (Q77) Osteochondrodysplasia with defects of growth of tubular bones and spine
  - (Q770) Achondrogenesis
  - (Q771) Thanatophoric short stature
  - (Q772) Short rib syndrome
  - (Q773) Chondrodysplasia punctata
  - (Q774) Achondroplasia
    - Hypochondroplasia
  - (Q775) Dystrophic dysplasia
  - (Q776) Chondroectodermal dysplasia
    - Ellis-van Creveld syndrome
  - (Q777) Spondyloepiphyseal dysplasia
  - (Q778) Other osteochondrodysplasia with defects of growth of tubular bones and spine
  - (Q779) Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified

- (Q78) Other osteochondrodysplasias
  - (Q780) Osteogenesis imperfecta
  - (Q781) Polyostotic fibrous dysplasia
  - (Q782) Osteopetrosis
  - (Q783) Progressive diaphyseal dysplasia
  - (Q784) Enchondromatosis
  - (Q785) Metaphyseal dysplasia
  - (Q786) Multiple congenital exostoses
  - (Q788) Other specified osteochondrodysplasias
  - (Q789) Osteochondrodysplasia, unspecified

- (Q79) Congenital malformations of the musculoskeletal system, not elsewhere classified
  - (Q790) Congenital diaphragmatic hernia
  - (Q791) Other congenital malformations of diaphragm
  - (Q792) Exomphalos
  - (Q793) Gastroschisis
  - (Q794) Prune belly syndrome
  - (Q795) Other congenital malformations of abdominal wall
  - (Q796) Ehlers-Danlos syndrome
  - (Q798) Other congenital malformations of musculoskeletal system
  - (Q799) Congenital malformation of musculoskeletal system, unspecified

### [แก้] (Q80-Q89) Other

- (Q80) Congenital ichthyosis
  - (Q800) Ichthyosis vulgaris
  - (Q801) X-linked ichthyosis
  - (Q804) Harlequin fetus
- (Q81) Epidermolysis bullosa
- (Q82) Other congenital malformations of skin
  - (Q821) Xeroderma pigmentosum
  - (Q822) Mastocytosis
    - Urticaria pigmentosa
  - (Q825) Congenital non-neoplastic naevus
    - Port-wine stain
- (Q83) Congenital malformations of breast
- (Q84) Other congenital malformations of integument
- (Q85) Phakomatoses, not elsewhere classified
  - (Q850) Neurofibromatosis (nonmalignant)
    - Von Recklinghausen's disease
  - (Q851) Tuberous sclerosis
    - Bourneville's disease
  - (Q858) Other phakomatoses, not elsewhere classified
    - Sturge-Weber syndrome
    - von Hippel-Lindau disease
- (Q86) Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
  - (Q860) Fetal alcohol syndrome (dysmorphic)
- (Q87) Other specified congenital malformation syndromes affecting multiple systems
  - (Q870) Congenital malformation syndromes predominantly affecting facial appearance
    - Mobius syndrome
  - (Q871) Congenital malformation syndromes predominantly associated with short stature
    - Prader-Willi syndrome
  - (Q872) Congenital malformation syndromes predominantly involving limbs
    - Klippel-Trénaunay-Weber
    - Rubinstein-Taybi syndrome
  - (Q873) Congenital malformation syndromes involving early overgrowth
    - Beckwith-Wiedemann syndrome
  - (Q874) Marfan's syndrome
  - (Q875) Other congenital malformation syndromes with other skeletal changes
  - (Q878) Other specified congenital malformation syndromes, not elsewhere classified
    - Zellweger's syndrome
    - Bardet-Biedl syndrome
- (Q89) Other congenital malformations, not elsewhere classified
  - (Q893) Situs inversus
  - (Q894) Conjoined twins

## [แก้] Q90-Q99 - Chromosomal abnormalities, not elsewhere classified

- (Q90) Down's syndrome
- (Q91) Trisomy 18 and Trisomy 13
- (Q92) Other trisomies and partial trisomies of the autosomes, not elsewhere classified
  - Trisomy 9
  - Warkany syndrome 2
- (Q93) Monosomies and deletions from the autosomes, not elsewhere classified
  - (Q933) Deletion of short arm of chromosome 4
    - Wolff-Hirschorn syndrome
  - (Q934) Deletion of short arm of chromosome 5
    - Cri-du-chat syndrome
  - (Q935) Other deletions of part of a chromosome
    - Angelman syndrome
- (Q95) Balanced rearrangements and structural markers, not elsewhere classified
  - Robertsonian and balanced reciprocal translocations and insertions
- (Q96) Turner syndrome
- (Q97) Other sex chromosome abnormalities, female phenotype, not elsewhere classified
  - (Q970) Karyotype 47,XXX
- (Q98) Other sex chromosome abnormalities, male phenotype, not elsewhere classified
  - (Q980) Klinefelter's syndrome karyotype 47,XXY
  - (Q985) Karyotype 47,XYY
- (Q99) Other chromosome abnormalities, not elsewhere classified
  - (Q992) Fragile X chromosome
    - Fragile X syndrome

## [แก้] ดูเพิ่ม

- รายการอาการในรหัส ICD-10 (List of ICD-10 codes)
- การจำแนกประเภทของโรคตามสถิติและปัญหาสาธารณะสุขสัมพันธ์ระหว่างประเทศ (International Statistical Classification of Diseases and Related Health Problems)

| ICD-10 บท Q: รูปวิปริตแต่กำเนิด การแปลงรูปและโครโมโซมผิดปกติ เป็นบทความเกี่ยวกับ การแพทย์ ที่ยังไม่สมบูรณ์ ต้องการตรวจสอบ เพิ่มเนื้อหา หรือเพิ่มแหล่งอ้างอิง คุณสามารถช่วยเพิ่มเติมหรือแก้ไข เพื่อให้สมบูรณ์มากขึ้น ข้อมูลเกี่ยวกับ ICD-10 บท Q: รูปวิปริตแต่กำเนิด การแปลงรูปและโครโมโซมผิดปกติ ในภาษาอื่น อาจสามารถหาอ่านได้จากเมนู ภาษาอื่น ด้านซ้ายมือ

ดึงข้อมูลจาก "http://th.wikipedia.org../../../%E0%B8%A3/%E0%B8%B9/%E0%B8%9B/ICD-10_%E0%B8%9A%E0%B8%97_Q%7E_%E0%B8%A3%E0%B8%B9%E0%B8%9B%E0%B8%A7%E0%B8%B4%E0%B8%9B%E0%B8%A3%E0%B8%B4%E0%B8%95%E0%B9%81%E0%B8%95%E0%B9%88%E0%B8%81%E0%B8%B3%E0%B9%80%E0%B8%99%E0%B8%B4%E0%B8%94_%E0%B8%81%E0%B8%B2%E0%B8%A3%E0%B9%81%E0%B8%9B%E0%B8%A5%E0%B8%87%E0%B8%A3%E0%B8%B9%E0%B8%9B%E0%B9%81%E0%B8%A5%E0%B8%B0%E0%B9%82%E0%B8%84%E0%B8%A3%E0%B9%82%E0%B8%A1%E0%B9%82%E0%B8%8B%E0%B8%A1%E0%B8%9C%E0%B8%B4%E0%B8%94%E0%B8%9B%E0%B8%81%E0%B8%95%E0%B8%B4_659a.html".

หมวดหมู่: บทความเกี่ยวกับ การแพทย์ ที่ยังไม่สมบูรณ์ | คู่มือการแพทย์

##### Views

- บทความ
- อภิปราย
- รุ่นปัจจุบัน

##### ค้นหา

##### ภาษาอื่น

- English