2026 ICD-10-CM Diagnosis Code Q72.30Congenital absence of unspecified foot and toe(s)
ICD-10-CM Codes›Q00-Q99›Q65-Q79›Q72
- Billable — Valid for Submission
- POA Exempt
- Chronic Condition
Q72.30 is a billable ICD-10-CM diagnosis code for congenital absence of unspecified foot and toe(s). It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 564 through 566. The code is exempt from POA reporting. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Musculoskeletal congenital conditions.
Code Identity
Code Classification
Present on Admission (POA)Billing
Q72.30 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review other POA exempt codes.
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Agenesis of calcaneus
- Agenesis of distal phalanx of second toe
- Agenesis of distal phalanx of third toe
- Agenesis of entire toe and metatarsal bone
- Agenesis of epiphysis of distal phalanx of fifth toe
- Agenesis of epiphysis of distal phalanx of fourth toe
- Agenesis of epiphysis of distal phalanx of great toe
- Agenesis of epiphysis of distal phalanx of second toe
- Agenesis of epiphysis of distal phalanx of third toe
- Agenesis of epiphysis of first metatarsal bone
- Agenesis of epiphysis of middle phalanx of fifth toe
- Agenesis of epiphysis of middle phalanx of fourth toe
- Agenesis of epiphysis of middle phalanx of second toe
- Agenesis of epiphysis of middle phalanx of third toe
- Agenesis of epiphysis of phalanx of toe
- Agenesis of epiphysis of proximal phalanx of fifth toe
- Agenesis of epiphysis of proximal phalanx of fourth toe
- Agenesis of epiphysis of proximal phalanx of great toe
- Agenesis of epiphysis of proximal phalanx of second toe
- Agenesis of epiphysis of proximal phalanx of third toe
- Agenesis of fifth metatarsal
- Agenesis of first metatarsal
- Agenesis of foot
- Agenesis of fourth and fifth metatarsals
- Agenesis of middle phalanx of third toe
- Agenesis of multiple metatarsal bones
- Agenesis of multiple tarsal bones
- Agenesis of proximal phalanx of third toe
- Agenesis of talus
- Agenesis of tarsal bone
- Agenesis of tarsal bone and metatarsal bone
- Aplasia of distal phalanx of fifth toe
- Aplasia of distal phalanx of foot
- Aplasia of distal phalanx of fourth toe
- Aplasia of distal phalanx of great toe
- Aplasia of distal phalanx of second toe
- Aplasia of distal phalanx of third toe
- Aplasia of great toe
- Aplasia of middle phalanx of fifth toe
- Aplasia of middle phalanx of foot
- Aplasia of middle phalanx of fourth toe
- Aplasia of middle phalanx of second toe
- Aplasia of middle phalanx of third toe
- Aplasia of phalanx of fifth toe
- Aplasia of phalanx of foot
- Aplasia of phalanx of fourth toe
- Aplasia of phalanx of great toe
- Aplasia of phalanx of second toe
- Aplasia of phalanx of third toe
- Aplasia of proximal phalanx of fifth toe
- Aplasia of proximal phalanx of foot
- Aplasia of proximal phalanx of fourth toe
- Aplasia of proximal phalanx of great toe
- Aplasia of proximal phalanx of second toe
- Aplasia of proximal phalanx of third toe
- Aplasia of toe
- Complete aphalangia of lower limb
- Congenital abnormal shape of tarsal bone
- Congenital absence of calcaneus
- Congenital absence of fifth toe
- Congenital absence of foot
- Congenital absence of fourth and fifth toes
- Congenital absence of great toe
- Congenital absence of metatarsal bone
- Congenital absence of multiple toes
- Congenital absence of talus
- Congenital absence of tarsal bone
- Congenital absence of toe
- Congenital anomaly of talus
- Longitudinal deficiency of foot
- Longitudinal deficiency of tarsal bone
- Partial aphalangia of lower limb
- Transverse arrest phalangeal level fifth ray
- Transverse arrest phalangeal level first ray
- Transverse arrest phalangeal level fourth ray
- Transverse arrest phalangeal level second ray
- Transverse arrest phalangeal level third ray
- Transverse deficiency lower limb - metatarsal level
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Patient EducationClinical
Birth Defects
A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.
The full article covers:
- What are birth defects?
- What causes birth defects?
- Who is at risk of having a baby with birth defects?
- How are birth defects diagnosed?
- What are the treatments for birth defects?
- Can birth defects be prevented?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert Q72.30 to ICD-9-CMHistory
Code HistoryHistory
Questions About Q72.30Overview
Is Q72.30 (Congenital absence of foot and toe(s)) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report congenital absence of unspecified foot and toe(s) on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does Q72.30 group to?
When congenital absence of unspecified foot and toe(s) is the principal diagnosis on an inpatient stay, it groups to MS-DRG 564, 565, 566, with relative weights from 0.7493 to 1.5436 depending on complications. Higher weights mean higher Medicare reimbursement.
Is Q72.30 exempt from POA reporting?
Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for congenital absence of unspecified foot and toe(s) on inpatient claims.
What is the ICD-9 equivalent of Q72.30?
Under the General Equivalence Mappings, congenital absence of unspecified foot and toe(s) converts to ICD-9-CM 755.38 (longitudinal defic foot) and 755.39 (longitud defic phalanges). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
