K00.9
BillableDisorder of tooth development, unspecified
Disorder of tooth development, unspecified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Disorder of odontogenesis NOS
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- embedded and impacted teeth (K01.-)
Also Known As / Clinical Terms
SNOMED CT
- Enamel projection109459007
- Enamel spur109459007
- Hyperpigmentation of oral mucosa235038002
- Melanin pigmentation of oral mucosa235038002
- Abnormal tooth development371136004
- Disorder of tooth development371136004
- Developmental abnormality of tooth size and form422775003
- Malformation of tooth422775003
- Tooth malformation422775003
- Congenital anomaly of tooth422977003
- Congenital malformation of tooth422977003
- CODAS (cerebro-oculo-dento-auriculo-skeletal) syndrome717772000
- CODAS syndrome717772000
- Cerebro-oculo-dento-auriculo-skeletal syndrome717772000
- Bork syndrome719910004
- Tricho-retino-dento-digital syndrome719910004
- Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome719910004
- Melanosis of mucosa of body orifice724847001
- Mucosal melanosis724847001
- Ectodermal dysplasia short stature syndrome764995008
- Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome764995008
- Short stature, nail dysplasia, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome764995008
- Spondyloepimetaphyseal dysplasia, abnormal dentition syndrome773302000
- Oligodontia787414001
- Selective tooth agenesis787414001
- Developmental abnormality of molar tooth1055322000
- Developmental abnormality of premolar tooth1055323005
- Developmental abnormality of incisor tooth1055324004
- Developmental abnormality of canine tooth1055325003
- Development abnormality of primary tooth1055326002
- Developmental abnormality of deciduous tooth1055326002
- Malformation of teeth1162865004
- Teeth malformation1162865004
Frequently Asked Questions
What is ICD-10 code K00.9?
ICD-10-CM code K00.9 represents "Disorder of tooth development, unspecified". It is a billable/specific code that can be used on a claim.
Is K00.9 a billable code?
Yes, K00.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is K00.9 in?
K00.9 is in Chapter 11: Diseases of the Digestive System (codes K00-K95).
What SNOMED CT codes does K00.9 map to?
K00.9 maps to 17 SNOMED CT concepts: 371136004, 719910004, 717772000, 422977003, 1055326002, and 12 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for K00.9?
K00.9 is linked to 1 UMLS Concept Unique Identifier: C0494698. 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.