Q74.9
BillableUnspecified congenital malformation of limb(s)
Unspecified congenital malformation of limb(s)
Status
Billable / Specific
Parent Code
Q74Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital anomaly of limb(s) NOS
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Micrognathia-glossoptosis syndrome4602007
- Pierre Robin association4602007
- Pierre Robin syndrome4602007
- Robin sequence4602007
- Increased platelets6631009
- Thrombocythaemia6631009
- Thrombocythemia6631009
- Thrombocytosis6631009
- VACTEL syndrome6839008
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects (VACTEL) syndrome6839008
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome6839008
- CDH - Congenital diaphragmatic hernia17190001
- Congenital diaphragmatic hernia17190001
- Eyes wide apart22006008
- Eyes widely set22006008
- Hypertelorism22006008
- Orbital hypertelorism22006008
- Orbital separation excessive22006008
- Triangular skull28740008
- Trigonocephalia28740008
- Trigonocephalus28740008
- Trigonocephaly28740008
- Akinesia33994004
- Congenital splenomegaly36752001
- Congenital hypotrichia56558005
- Congenital hypotrichosis56558005
- Hypotrichosis congenita56558005
- Congenital abnormality of the limb60475009
- Congenital anomaly of limb60475009
- Congenital deformity of limb60475009
- Splenogonadal fusion62042001
- Arachnodactyly62250003
- Congenital arachnodactyly62250003
- Spider finger62250003
- Facial-limb disruptive spectrum89444000
- Hypoglossia-hypodactyly syndrome89444000
- Oromandibular-limb hypogenesis spectrum89444000
- Congenital abnormal shape of frontal bone92912009
- Congenital misshapen frontal bone92912009
- Congenital anomaly of joint95463009
- Congenital articular malformation95463009
- Congenital joint malformation95463009
- Cleft nose204521002
- Congenital cleft nose204521002
- Brachymesophalangia205317004
- Multiple pterygium syndrome205819008
- Non-anaemic red cell disorder234338001
- Non-anemic red cell disorder234338001
- Macrocytosis - no anaemia234339009
- Macrocytosis - no anemia234339009
- Cardio-acral-facial syndrome403769007
- Rabenhorst syndrome403769007
- Congenital anomaly of digit403855001
- Congenital malformation of digit403855001
- Developmental anomaly of digits403855001
- Perodactylia403855001
- Platelet count above reference range415115007
- VACTERL syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects (VACTERL) syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects (VACTERL) syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects syndrome431395004
- Craniofacial deafness hand syndrome702362004
- Sommer Young Wee Frye syndrome702362004
- Feingold syndrome702431004
- Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome702431004
- Microcephaly-oculo-digito-esophageal-duodenal syndrome702431004
- Microcephaly-oculo-digito-oesophageal-duodenal syndrome702431004
- Oculo-digito-esophagoduodenal syndrome702431004
- Oculo-digito-oesophagoduodenal syndrome702431004
- Diaphragmatic hernia, abnormal face and distal limb anomalies702432006
- Fryns syndrome702432006
- Cranio-facio-digito-genital syndrome716089008
- Craniofacial digital and genital anomalies syndrome716089008
- Harrod syndrome716089008
- Mullerian duct and limb anomalies syndrome716111003
- MDN (mammary digital nail) syndrome718679004
- Mammary digital nail syndrome718679004
- Onycho-digito-mammary syndrome718679004
- Oral-facial-digital syndrome type 9718680001
- Oro-facial digital syndrome type 9718680001
- Orofaciodigital syndrome type 9718680001
- Orofaciodigital syndrome with retinal abnormality718680001
- Oral-facial-digital syndrome Gabrielli type718681002
- Oral-facial-digital syndrome type 11718681002
- Oro-facial digital syndrome type 11718681002
- Orofaciodigital syndrome Gabrielli type718681002
- Orofaciodigital syndrome type 11718681002
- VACTERL syndrome with hydrocephalus719043002
- Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus719043002
- Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-oesophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus719043002
- Renal dysplasia with limb defect syndrome719840003
- Renal dysplasia, mesomelia, radiohumeral fusion syndrome719840003
- Ulbright Hodes syndrome719840003
- Trigonocephaly with bifid nose and acral anomaly syndrome719948009
- Acro-renal-mandibular syndrome720414005
- Acrorenal mandibular syndrome720414005
- Split hand and split foot with mandibular hypoplasia syndrome720414005
- Acrofacial dysostosis Catania type720419000
- Opitz Caltabiano syndrome720419000
- Brachytelephalangy, facial dysmorphism, Kallmann syndrome720574003
- Bakrania Ragge syndrome721878003
- Microphthalmia with brain and digit anomaly721878003
- Syndromic microphthalmia type 6721878003
- Figuera syndrome722075004
- Oro-facial digital syndrome type 10722075004
- Orofaciodigital syndrome type 10722075004
- Orofaciodigital syndrome with fibular aplasia722075004
- Oro-facial digital syndrome type 5722105002
- Orofaciodigital syndrome Thurston type722105002
- Orofaciodigital syndrome type 5722105002
- Thurston syndrome722105002
- EE - epileptic encephalopathy723125008
- Epileptic encephalopathy723125008
- Chitayat Meunier Hodgkinson syndrome723461007
- Pierre Robin sequence faciodigital anomaly syndrome723461007
- Pierre Robin sequence with facial and digital anomalies723461007
- Braun Bayer syndrome724092009
- Nephrosis, deafness, urinary tract, digital malformation syndrome724092009
- Aarskog-like syndrome725434009
- Autosomal recessive facio-digito-genital syndrome725434009
- Autosomal recessive faciodigitogenital syndrome725434009
- Facio-digito-genital syndrome Kuwait type725434009
- Teebi Naguib Alawadi syndrome725434009
- Freire Maia Pinheiro Opitz syndrome725908007
- NFDR (neurofaciodigitorenal) syndrome725908007
- Neurofaciodigitorenal syndrome725908007
- SGFLD (splenogonadal fusion limb defect syndrome) syndrome726724005
- Splenogonadal fusion limb defect syndrome726724005
- Splenogonadal fusion, limb defect, micrognathia syndrome726724005
- Clayton-Smith Donnai syndrome732950006
- Ichthyosis, oral and digital anomalies syndrome732950006
- Charlie M syndrome733034007
- OSLAM (osteosarcoma, limb anomalies, erythroid macrocytosis) syndrome733064004
- OSLAM syndrome733064004
- Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome733064004
- Microcephaly, cerebral malformation, orofaciodigital syndrome763837007
- Oro-facial digital syndrome type 14763837007
- Orofaciodigital syndrome type 14763837007
- Cleft lip, limb and heart malformation syndrome764697003
- Verloove Vanhorick Brubakk syndrome764697003
- Familial thrombocytosis with transverse limb defect771511005
- Hereditary thrombocytosis with transverse limb defect771511005
- Thrombocythaemia with distal limb defect771511005
- Thrombocythemia with distal limb defect771511005
- DSS - disproportionate short stature772086000
- Disproportionate short stature772086000
- Emery Nelson syndrome773768000
- Hand and foot deformity, flat facies syndrome773768000
- Bifid nose787413007
- Abnormally short little finger897328006
- Shortened little finger897328006
- Lethal congenital SLSS (short limb short stature)926342004
- Lethal congenital disproportionate short limbed short stature926342004
- Lethal congenital short limb short stature926342004
- Microphthalmos due to Fryns syndrome1003370000
- Hypoplasia of distal phalanx of foot1144708001
- Hypoplasia of distal phalanx of toe1144708001
- OFD18 - oral-facial-digital syndrome type 181177179002
- Oral-facial-digital syndrome with short stature and brachymesophalangia1177179002
- Orofaciodigital syndrome type 181177179002
- Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome1187042007
- Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies1208985003
- RHOA (ras homolog family member A) related mosaic ectodermal dysplasia1208985003
- RHOA-related mosaic ectodermal dysplasia1208985003
- TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome1208998007
- Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome1208998007
- Tumour necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome1208998007
- Agammaglobulinaemia due to TOP2B mutation1230295000
- Agammaglobulinemia due to TOP2B mutation1230295000
- B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome1230295000
- BILU (B-cell immunodeficiency, limb, urogenital) syndrome1230295000
- BILU syndrome1230295000
- Hoffman syndrome due to TOP2B deficiency1230295000
- DNA replication fork stabilisation factor DONSON-related microcephaly, short stature, limb abnormalities spectrum1236845001
- DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum1236845001
- DONSON-related microcephaly, short stature, limb abnormalities spectrum1236845001
- Mesomelic dysplasia, digital anomalies, intellectual disability syndrome1363286000
- Congenital dysplasia of limb88631000119105
UMLS
- CONGEN LIMB DEFORMITIESC0206762
- Congenital Limb DeformitiesC0206762
- Congenital Limb DeformityC0206762
- Congenital abnormality of the limbC0206762
- Congenital anomaly of limbC0206762
- Congenital anomaly of limb (disorder)C0206762
- Congenital anomaly of limb(s) NOSC0206762
- Congenital deformity of limbC0206762
- Congenital limb anomaly NOSC0206762
- Congenital limb malformation NOSC0206762
- Deformities, Congenital LimbC0206762
- Deformity, Congenital LimbC0206762
- LIMB DEFORMITIES CONGENC0206762
- Limb Deformities, CongenitalC0206762
- Limb Deformity, CongenitalC0206762
- Limb malformationC0206762
- Limb malformation NOSC0206762
- Limb malformationsC0206762
- Unspecified congenital malformation of limb(s)C0206762
- limb malformationC0206762
- limb malformationsC0206762
- limbs malformationC0206762
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.
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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.