DONSON-related microcephaly, short stature, limb abnormalities spectrum
Congenital limb anomaly NOS
Tumour necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
Microphthalmos due to Fryns syndrome
Mullerian duct and limb anomalies syndrome
Deformity, Congenital Limb
SGFLD (splenogonadal fusion limb defect syndrome) syndrome
Syndromic microphthalmia type 6
EE - epileptic encephalopathy
Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome
Congenital abnormal shape of frontal bone
Familial thrombocytosis with transverse limb defect
Orbital separation excessive
Trigonocephaly with bifid nose and acral anomaly syndrome
Arachnodactyly
Brachymesophalangia
Congenital limb malformation NOS
Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus
Multiple pterygium syndrome
BILU (B-cell immunodeficiency, limb, urogenital) syndrome
Macrocytosis - no anemia
Congenital misshapen frontal bone
Neurofaciodigitorenal syndrome
Thrombocytosis
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects syndrome
VACTERL syndrome
Macrocytosis - no anaemia
Orofaciodigital syndrome type 10
OSLAM (osteosarcoma, limb anomalies, erythroid macrocytosis) syndrome
Splenogonadal fusion limb defect syndrome
Trigonocephaly
Orofaciodigital syndrome with retinal abnormality
Congenital Limb Deformity
Akinesia
Limb malformation
Feingold syndrome
Oral-facial-digital syndrome with short stature and brachymesophalangia
CONGEN LIMB DEFORMITIES
Hoffman syndrome due to TOP2B deficiency
Opitz Caltabiano syndrome
Non-anaemic red cell disorder
Agammaglobulinaemia due to TOP2B mutation
Oro-facial digital syndrome type 5
Splenogonadal fusion, limb defect, micrognathia syndrome
Congenital abnormality of the limb
VACTEL syndrome
Lethal congenital short limb short stature
Cardio-acral-facial syndrome
Cleft lip, limb and heart malformation syndrome
Nephrosis, deafness, urinary tract, digital malformation syndrome
Eyes wide apart
Spider finger
Congenital dysplasia of limb
Congenital hypotrichosis
Hypoplasia of distal phalanx of foot
Thrombocythemia
Verloove Vanhorick Brubakk syndrome
OFD18 - oral-facial-digital syndrome type 18
Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
Trigonocephalia
Mammary digital nail syndrome
Hypotrichosis congenita
Oro-facial digital syndrome type 14
Ulbright Hodes syndrome
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects (VACTEL) syndrome
Autosomal recessive facio-digito-genital syndrome
Disproportionate short stature
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome
Congenital splenomegaly
DSS - disproportionate short stature
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects (VACTERL) syndrome
limb malformations
Bakrania Ragge syndrome
Robin sequence
Thrombocythemia with distal limb defect
Congenital arachnodactyly
Cleft nose
Deformities, Congenital Limb
Orofaciodigital syndrome type 11
Craniofacial deafness hand syndrome
Oculo-digito-esophagoduodenal syndrome
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects (VACTERL) syndrome
Charlie M syndrome
Lethal congenital disproportionate short limbed short stature
Pierre Robin sequence with facial and digital anomalies
Microcephaly-oculo-digito-oesophageal-duodenal syndrome
OSLAM syndrome
Onycho-digito-mammary syndrome
Congenital Limb Deformities
Ichthyosis, oral and digital anomalies syndrome
Platelet count above reference range
Shortened little finger
Clayton-Smith Donnai syndrome
Orofaciodigital syndrome type 14
Orofaciodigital syndrome type 9
Orbital hypertelorism
VACTERL syndrome with hydrocephalus
Non-anemic red cell disorder
Trigonocephalus
Split hand and split foot with mandibular hypoplasia syndrome
Pierre Robin sequence faciodigital anomaly syndrome
Congenital articular malformation
Eyes widely set
Oro-facial digital syndrome type 9
Acro-renal-mandibular syndrome
Bifid nose
Thrombocythaemia with distal limb defect
Limb malformation NOS
Orofaciodigital syndrome Thurston type
Congenital hypotrichia
Increased platelets
Microcephaly, cerebral malformation, orofaciodigital syndrome
Congenital anomaly of digit
Acrorenal mandibular syndrome
Acrofacial dysostosis Catania type
Agammaglobulinemia due to TOP2B mutation
Epileptic encephalopathy
Congenital cleft nose
Hypertelorism
Congenital anomaly of limb (disorder)
Facio-digito-genital syndrome Kuwait type
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
RHOA (ras homolog family member A) related mosaic ectodermal dysplasia
TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
Perodactylia
Hereditary thrombocytosis with transverse limb defect
Hypoplasia of distal phalanx of toe
Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-oesophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus
Developmental anomaly of digits
Emery Nelson syndrome
Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome
RHOA-related mosaic ectodermal dysplasia
Chitayat Meunier Hodgkinson syndrome
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome
Braun Bayer syndrome
Triangular skull
Congenital anomaly of limb(s) NOS
Sommer Young Wee Frye syndrome
Abnormally short little finger
Teebi Naguib Alawadi syndrome
Congenital deformity of limb
MDN (mammary digital nail) syndrome
Diaphragmatic hernia, abnormal face and distal limb anomalies
Pierre Robin association
Orofaciodigital syndrome Gabrielli type
BILU syndrome
Rabenhorst syndrome
Microphthalmia with brain and digit anomaly
Oral-facial-digital syndrome type 9
Oro-facial digital syndrome type 11
Oral-facial-digital syndrome type 11
Brachytelephalangy, facial dysmorphism, Kallmann syndrome
Autosomal recessive faciodigitogenital syndrome
Mesomelic dysplasia, digital anomalies, intellectual disability syndrome
Orofaciodigital syndrome with fibular aplasia
LIMB DEFORMITIES CONGEN
Harrod syndrome
Aarskog-like syndrome
Splenogonadal fusion
Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome
Hand and foot deformity, flat facies syndrome
Microcephaly-oculo-digito-esophageal-duodenal syndrome
Freire Maia Pinheiro Opitz syndrome
Fryns syndrome
Orofaciodigital syndrome type 18
Craniofacial digital and genital anomalies syndrome
Thurston syndrome
Congenital anomaly of joint
limbs malformation
Limb Deformities, Congenital
Oromandibular-limb hypogenesis spectrum
Lethal congenital SLSS (short limb short stature)
Figuera syndrome
NFDR (neurofaciodigitorenal) syndrome
Facial-limb disruptive spectrum
Oro-facial digital syndrome type 10
Congenital joint malformation
DNA replication fork stabilisation factor DONSON-related microcephaly, short stature, limb abnormalities spectrum
Limb Deformity, Congenital
Hypoglossia-hypodactyly syndrome
Oculo-digito-oesophagoduodenal syndrome
CDH - Congenital diaphragmatic hernia
Congenital anomaly of limb
Pierre Robin syndrome
Congenital diaphragmatic hernia
Cranio-facio-digito-genital syndrome
Micrognathia-glossoptosis syndrome
Oral-facial-digital syndrome Gabrielli type
Renal dysplasia, mesomelia, radiohumeral fusion syndrome
Thrombocythaemia
Congenital malformation of digit
Renal dysplasia with limb defect syndrome
Orofaciodigital syndrome type 5
DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum

Frequently Asked Questions

What is the ICD-10 code for unspecified congenital malformation of limb(s)?

The ICD-10-CM code for unspecified congenital malformation of limb(s) is Q74.9. The full clinical description is "Unspecified congenital malformation of limb(s)". Q74.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q74.9 mean?

ICD-10-CM code Q74.9 represents “Unspecified congenital malformation of limb(s)”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q74.9 a billable code?

Yes, Q74.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q74.9 in?

Q74.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q74.9?

Q74.9 has Excludes1 notes indicating codes that cannot be used together with it, including: polydactyly (Q69.-); reduction defect of limb (Q71-Q73); syndactyly (Q70.-).

What SNOMED CT codes does Q74.9 map to?

Q74.9 maps to 68 SNOMED CT concepts: 725434009, 897328006, 720414005, 720419000, 1230295000, and 63 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q74.9?

Q74.9 is linked to 1 UMLS Concept Unique Identifier: C0206762. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q74.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like unspecified congenital malformation of limb(s) affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q74.9?

Q74.9 maps to the ICD-11 code: LB9Z (Structural developmental anomalies of the skeleton, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.