ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities

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International Statistical Classification of Diseases and Related Health Problems 10th Revision
Chapter Blocks Title
I A00-B99 Certain infectious and parasitic diseases
II C00-D48 Neoplasms
III D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
IV E00-E90 Endocrine, nutritional and metabolic diseases
V F00-F99 Mental and behavioural disorders
VI G00-G99 Diseases of the nervous system
VII H00-H59 Diseases of the eye and adnexa
VIII H60-H95 Diseases of the ear and mastoid process
IX I00-I99 Diseases of the circulatory system
X J00-J99 Diseases of the respiratory system
XI K00-K93 Diseases of the digestive system
XII L00-L99 Diseases of the skin and subcutaneous tissue
XIII M00-M99 Diseases of the musculoskeletal system and connective tissue
XIV N00-N99 Diseases of the genitourinary system
XV O00-O99 Pregnancy, childbirth and the puerperium
XVI P00-P96 Certain conditions originating in the perinatal period
XVII Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities
XVIII R00-R99 Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified
XIX S00-T98 Injury, poisoning and certain other consequences of external causes
XX V01-Y98 External causes of morbidity and mortality
XXI Z00-Z99 Factors influencing health status and contact with health services
XXII U00-U99 Codes for special purposes
The International Statistical Classification of Diseases and Related Health Problems 10th Revision (ICD-10) is a coding of diseases and signs, symptoms, abnormal findings, complaints, social circumstances and external causes of injury or diseases, as classified by the World Health Organization (WHO).[1]. This page contains ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities.

Q00-Q89 - Congenital malformations and deformations

(Q00-Q07) nervous system

(Q10-Q18) eye, ear, face and neck

Eye

Ear

Other face and neck

(Q20-Q28) circulatory system

(Q30-Q34) respiratory system

(Q35-Q45) digestive system

(Q50-Q56) genital organs

(Q60-Q64) urinary system

(Q65-Q79) musculoskeletal system

(Q80-Q89) Other

Q90-Q99 - Chromosomal abnormalities, not elsewhere classified

See also

References

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Pathology: Medical conditions and ICD code
(Disease / Disorder / Illness, Syndrome / Sequence, Symptom / Sign, Injury, etc.)
(A/B, 001-139)
(C/D,
140-239 & 280-289)
(E, 240-278)
(F, 290-319)
(G, 320-359)
(H, 360-389)
(I, 390-459)
(J, 460-519)
(K, 520-579)
(L, 680-709)
(M, 710-739)
(N, 580-629)
(O, 630-679)
(P, 760-779)
(Q, 740-759)
(R, 780-799)
(S/T, 800-999)
Congenital malformations and deformations of nervous system (Q00-Q07, 740-742)
Brain
Other
Spinal cord
Other
Congenital malformations and deformations of eyes (Q10-Q15, 743)
Adnexa
Globe
Entire eye
Other

M: EYE

anat(g, a, p)/phys/devp/cell

proc, drug(S1A/1E/1F/1L)

Congenital malformations and deformations of ears (Q16-Q17, 744.0-744.3)
Size
Position
Other

M: EAR

anat(e, p)/phys/devp

proc, drug(S2)

Congenital malformations and deformations of face and neck (Q18, 744.4-744.9)
Face
Neck
Cardiac shunt/
heart septal defect
L→R and R→L: Eisenmenger's syndrome
R→L, with other conditions: Tetralogy of Fallot
Valvular heart disease/
heart chambers
Right
Left
Other
Great arteries/
other arteries
Great veins
Arteriovenous malformation
Congenital malformations and deformations of respiratory system (Q30-Q34, 748)
Upper RT
Lower RT

M: RES

anat(n, x, l, c)/phys/devp

proc, drug(R1/2/3/5/6/7)

Congenital malformations and deformations of digestive system (Q35-Q45, 749-751)
Upper GI tract
Lower GI tract
Accessory
Female congenital anomalies of the genitalia, including Intersex and DSD: (Q50-Q52 · 752.0-752.4)
Internal
External
Abdominal
Pelvic
Vestigial
Appendicular:
Limb/
dysmelia
Either/both
Axial

M: JNT

anat(h/c, u, t, l)/phys

proc, drug(M4)

Osteodysplasia/
osteodystrophy
Other/ungrouped
Chondrodysplasia/
chondrodystrophy
(including dwarfism)
Other dwarfism
Congenital diaphragm and abdominal wall defects, abdominopelvic cavity (Q79.0-Q79.5, 756.6-756.7)
Thoracic diaphragm
Abdominal wall

M: MUS, DF+DRCT

anat (h/n, u, t/d, a/p, l)/phys/hist

noco(m, s, c)/cong(d)/tumr, sysi/epon, injr

proc, drug (M1A/3)

Congenital malformations and deformations of integument (Q80-Q82, 757.0-757.3)
Skin disease/
genodermatosis
Ungrouped
Other
Elastic/Connective
Ungrouped cutaneous
congenital anomalies
With OMIM
Without OMIM
Accessory nail of the fifth toe · Arteriovenous fistula · Bronchogenic cyst · Congenital cartilaginous rest of the neck · Congenital hypertrophy of the lateral fold of the hallux · Congenital lip pit · Congenital malformations of the dermatoglyphs · Congenital preauricular fistula · Congenital smooth muscle hamartoma · Cystic lymphatic malformation · Dermoid cyst · Encephalocele · Infantile hemangioma · Malignant pilomatricoma · Median raphe cyst · Melanotic neuroectodermal tumor of infancy · Mongolian spot · Nasal glioma · Nasolacrimal duct cyst · Omphalomesenteric duct cyst · Pilomatricoma · Poland anomaly · PHACE association · Rapidly involuting congenital hemangioma · Rosenthal–Kloepfer syndrome · Rudimentary supernumerary digit · Sinus pericranii · Skin dimple · Superficial lymphatic malformation · Supernumerary nipple · Thyroglossal duct cyst · Verrucous vascular malformation
Ungrouped
genodermatoses
With OMIM
SLC39A4 (Acrodermatitis enteropathica) · ATP2A2 (Acrokeratosis verruciformis) · C20orf42 ( Kindler syndrome) · GNAS (Albright's hereditary osteodystrophy) · FGFR2 (Apert syndrome) · VPS33B (Arthrogryposis–renal dysfunction–cholestasis syndrome) · MRN complex ( Ataxia telangiectasia) · HR (Atrichia with papular lesions) · AIRE (Autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy syndrome)

deletion: 18q deletion syndrome · Angelman syndrome

genetics unknown: Acrogeria · Adams–Oliver syndrome · Adducted thumbs syndrome · Atrophodermia vermiculata

unsorted: Bart syndrome · Bazex–Dupré–Christol syndrome · Bloom syndrome · BIDS syndrome · Cardiofaciocutaneous syndrome · Cartilage–hair hypoplasia · Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome · Chondrodysplasia punctata · Cockayne syndrome · CHILD syndrome · Conradi–Hünermann syndrome · Costello syndrome · Cronkhite–Canada syndrome · Crouzon syndrome · Cutis verticis gyrata · DeSanctis–Cacchione syndrome · Dolichol kinase deficiency · Ectrodactyly–ectodermal dysplasia–cleft syndrome · Focal dermal hypoplasia · Franceschetti–Klein syndrome · Gardner's syndrome · Hallerman–Streiff syndrome · Hay–Wells syndrome · Hereditary sclerosing poikiloderma · IBIDS syndrome · Incontinentia pigmenti achromians · IPEX syndrome · Johanson–Blizzard syndrome · Johnson–McMillin syndrome · Joubert syndrome · Kabuki syndrome · Klippel–Feil syndrome · Lelis syndrome · Lenz–Majewski syndrome · Mandibuloacral dysplasia · Marinesco–Sjögren syndrome · Metageria · Multiple lentigines syndrome · Multiple sulfatase deficiency · Naegeli–Franceschetti–Jadassohn syndrome · Neurofibromatosis (Neurofibromatosis type 1, Neurofibromatosis type 3, Neurofibromatosis type 4, Segmental neurofibromatosis) · Neutral lipid storage disease · Noonan syndrome · Oculocerebrocutaneous syndrome · Oculodentodigital dysplasia · Odonto–Tricho–Ungual–Digital–Palmar syndrome · Oliver–McFarlane syndrome · Pachydermoperiostosis · Peeling skin syndrome · Pfeiffer syndrome · Popliteal pterygium syndrome · Porokeratosis (Porokeratosis palmaris et plantaris disseminata, Craniosynostosis–anal anomalies–porokeratosis syndrome, Disseminated superficial actinic porokeratosis, Disseminated superficial porokeratosis, Linear porokeratosis, Plaque-type porokeratosis, Punctate porokeratosis) · Prader–Willi syndrome · Progeria · Progressive osseous heteroplasia · Progressive symmetric erythrokeratodermia · Proteus syndrome · Rapp–Hodgkin syndrome · Refsum's disease · Restrictive dermopathy · Rhizomelic chondrodysplasia punctata · Rombo syndrome · Rothmund–Thomson syndrome · Rud syndrome · Say syndrome · Scalp–ear–nipple syndrome · Schindler disease · Schinzel–Giedion syndrome · Scleroatrophic syndrome of Huriez · Senter syndrome · Shabbir syndrome · Silver–Russell syndrome · Skin fragility syndrome · Terminal osseous dysplasia with pigmentary defects · Tooth and nail syndrome · Townes–Brocks syndrome · Transient bullous dermolysis of the newborn · Treacher Collins syndrome · Tricho–rhino–phalangeal syndrome · Tuberous sclerosis · Ulnar–mammary syndrome · Van Der Woude syndrome · Von Hippel–Lindau syndrome · Watson syndrome · Werner syndrome · Westerhof syndrome · Whistling syndrome · Wilson–Turner syndrome · Wolf–Hirschhorn syndrome · X-linked recessive chondrodysplasia punctata · Zimmermann–Laband syndrome
Without OMIM

M: INT, SF, LCT

noco(i/b/d/q/u/r/p/m/k/v/f)/cong/tumr(n/e/d), sysi/epon

proc, drug (D2/3/4/5/8/11)

Congenital malformations and deformations of skin appendages (Q84, 757.4-757.5)
Nail disease
Hair disease
Congenital malformations and deformations of the breast (Q83, 757.6)
Breast
Nipple
Neurofibromatosis
Angiomatosis
Hamartoma
Other
Congenital malformation due to exogenous toxicity (Q86, 760.7)
Alcohol
Other
Congenital abnormality · multiple abnormalities (Q87, 759.7)
Craniofacial
Short stature
Limbs
Overgrowth
Laurence-Moon-Bardet-Biedl
Combined/other,
known locus
Acquired
Congenital
Pancreas
Hypothalamic/
pituitary axes
+parathyroid
Zygosity
Monochorionic twins
Conjoined twins
Other
Pathology: chromosome abnormalities (Q90-Q99 · 758)
Autosomal
X/Y linked
Translocations
Lymphoid
Myeloid
Other
Gonadal dysgenesis
Other
es:Anexo:CIE-10 Capítulo XVII: Malformaciones congénitas, deformidades y anomalías cromosómicas

hr:MKB-10 poglavlje XVII: Prirođene malformacije, deformacije i kromosomske abnormalnosti hu:BNO-10-17 – Veleszületett rendellenességek, deformitások és kromoszómaabnormitások no:ICD-10 kapittel XVII: Q00-Q99 - Medfødte misdannelser, deformiteter og kromosomavvik ru:МКБ-10: Класс XVII sh:MKB-10 Poglavlje XVII: Urođene malformacije, deformacije i hromozomske abnormalnosti fi:ICD-10-pääluokka Q te:ICD-10 అధ్యాయము 17: వంశపారంపరిక అవలక్షణాలు మరియు జన్యు సంబంధ వ్యాధులు th:ICD-10 บทที่ 17: รูปผิดปกติแต่กำเนิด รูปพิการ และความผิดปกติของโครโมโซม tr:ICD-10, Bölüm 17 (Q00-Q99): Konjenital malformasyonlar, deformasyonlar ve kromozom anormallikleri uk:ICD-10 Розділ Q

zh:ICD-10 第十七章：先天畸形、变形和染色体异常
  1. ↑ WHO | International Classification of Diseases (ICD)
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