Q72.899
BillableOther reduction defects of unspecified lower limb
Other reduction defects of unspecified lower limb
Status
Billable / Specific
Parent Code
Q72.89Coding Notes
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
- Incomplete congenital absence of lower extremity16904009
- Incomplete congenital absence of lower limb16904009
- Incomplete congenital absence of thigh AND leg16904009
- Transverse arrest of the leg36574005
- Transverse deficiency of leg36574005
- Transverse deficiency of lower limb36574005
- Ectromelia43036001
- Ectromelia of lower limb52474000
- Congenital longitudinal deficiency lower limb66078008
- Congenital shortening of leg66078008
- Congenital undergrowth of lower limb66078008
- Congenital undergrowth of whole of lower limb66078008
- Hemimelia of lower limb66078008
- Longitudinal deficiency of lower limb66078008
- Leg reduction deformity77595004
- Reduction deformity of lower limb77595004
- Congenital abnormal shape of ilium92917003
- Congenital misshapen ilium92917003
- Congenital hypoplasia of femur93255008
- Congenital short femur93255008
- Congenital hypoplasia of fibula93256009
- Congenital short fibula93256009
- Congenital hypoplasia of tibia93298007
- Congenital short tibia93298007
- Congenital hypoplasia of ulna93300007
- Congenital short ulna93300007
- Transverse deficiency lower limb - through femur205206003
- Transverse deficiency lower limb - through tibia/fibula205207007
- Mesomelic dwarfism Reinhardt-Pfeiffer type715472000
- Mesomelic dysplasia of hypoplastic ulna and fibula type715472000
- Reinhardt Pfeiffer mesomelic dysplasia715472000
- Reinhardt Pfeiffer syndrome715472000
- Aplasia of fibula co-occurrent with complex brachydactyly715474004
- Du Pan syndrome715474004
- Fibular aplasia and complex brachydactyly715474004
- Brachymelia of leg717850006
- Brachymelia of lower limb717850006
- Absent tibia polydactyly syndrome764857004
- Tibial hemimelia, polysyndactyly, triphalangeal thumb syndrome764857004
- Radial deficiency, tibial hypoplasia syndrome783137003
- FATCO syndrome783156008
- Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome783156008
- Hecht Scott syndrome783156008
- Abnormally short ilium897494000
- Short iliac bone897494000
- Congenital hypoplasia of toe1144672005
- Hypoplasia of distal phalanx of third toe1144696000
- Congenital hypoplasia of middle phalanx of third toe1144698004
- Congenital hypoplasia of phalanx of third toe1144699007
- Congenital hypoplasia of proximal phalanx of third toe1144702000
- Congenital hypoplasia of first toe1144704004
- Congenital hypoplasia of great toe1144704004
- Congenital hypoplasia of hallux1144704004
- Congenital hypoplasia of phalanx of first toe1144705003
- Congenital hypoplasia of phalanx of great toe1144705003
- Congenital hypoplasia of phalanx of hallux1144705003
- Congenital hypoplasia of proximal phalanx of first toe1144706002
- Congenital hypoplasia of proximal phalanx of great toe1144706002
- Congenital hypoplasia of proximal phalanx of hallux1144706002
- Congenital hypoplasia of proximal phalanx of foot1144707006
- Congenital hypoplasia of proximal phalanx of toe1144707006
- Hypoplasia of distal phalanx of foot1144708001
- Hypoplasia of distal phalanx of toe1144708001
- Hypoplasia of distal phalanx of second toe1144710004
- Hypoplasia of distal phalanx of fourth toe1144711000
- Hypoplasia of distal phalanx of fifth toe1144712007
- Hypoplasia of distal phalanx of little toe1144712007
- Hypoplasia of distal phalanx of first toe1144713002
- Hypoplasia of distal phalanx of great toe1144713002
- Hypoplasia of distal phalanx of hallux1144713002
- Congenital hypoplasia of middle phalanx of foot1144714008
- Congenital hypoplasia of middle phalanx of toe1144714008
- Congenital hypoplasia of middle phalanx of second toe1144715009
- Congenital hypoplasia of middle phalanx of fourth toe1144716005
- Congenital hypoplasia of middle phalanx of fifth toe1144717001
- Congenital hypoplasia of middle phalanx of little toe1144717001
- Congenital hypoplasia of phalanx of second toe1144718006
- Congenital hypoplasia of phalanx of fourth toe1144719003
- Congenital hypoplasia of phalanx of fifth toe1144720009
- Congenital hypoplasia of phalanx of little toe1144720009
- Congenital hypoplasia of phalanx of foot1144721008
- Congenital hypoplasia of phalanx of toe1144721008
- Congenital hypoplasia of lesser trochanter of femur1145353005
- Congenital hypoplasia of bone of forearm1145430008
- Congenital hypoplasia of bone of radius and/or ulna1145430008
- Congenital hypoplasia of bone of head and neck of femur1145431007
- Congenital hypoplasia of capital epiphysis of femur1145434004
- Congenital hypoplasia of proximal epiphysis of femur1145434004
- Aplasia of fibula1145459008
- Mesomelic dysplasia of lower limb1263481007
Frequently Asked Questions
What is the ICD-10 code for other reduction defects of unspecified lower limb?
The ICD-10-CM code for other reduction defects of unspecified lower limb is Q72.899. The full clinical description is "Other reduction defects of unspecified lower limb". Q72.899 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q72.899 mean?
ICD-10-CM code Q72.899 represents "Other reduction defects of unspecified lower limb". 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 Q72.899 a billable code?
Yes, Q72.899 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q72.899 in?
Q72.899 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q72.899 map to?
Q72.899 maps to 48 SNOMED CT concepts: 897494000, 764857004, 1145459008, 715474004, 717850006, and 43 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q72.899?
Q72.899 is linked to 1 UMLS Concept Unique Identifier: C2977517. 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.