AutoICD API

K00.5

Billable

Hereditary disturbances in tooth structure, NEC

Hereditary disturbances in tooth structure, not elsewhere classified

Status

Billable / Specific

Block

K00-K14

Parent Code

K00

ICD-11 Mapping

1 equivalent

Coding Notes

Related Codes(9)
ICD-11 Equivalents(1)
Also Known As / Clinical Terms(247)

SNOMED CT

Clinical Terms

  • Radicular dentine dysplasia
  • Coronal dentine dysplasia
  • Hypomineralization of enamel of teeth
  • Goldblatt chondrodysplasia
  • Dermo-odonto dysplasia
  • Congenital abnormality of sclera
  • Osteosclerosis
  • Suarez Stickler syndrome
  • Amelogenesis imperfecta, hypomaturation type
  • Dentinogenesis imperfecta without osteogenesis imperfecta
  • Amelogenesis imperfecta, nephrocalcinosis and impaired renal concentration
  • dentinogenesis imperfecta
  • Anomalous dysplasia of dentine
  • dentinal dysplasia
  • Dysplasia, Dentin
  • Enamel renal syndrome
  • Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
  • Dermoodonto dysplasia
  • Dentin Dysplasia
  • Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency
  • Amelogenesis imperfecta - hypomaturation - snow capped teeth
  • Brachyolmia and amelogenesis imperfecta syndrome
  • Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth
  • Hypocalcification of teeth
  • Microdontia
  • Odontogenesis imperfecta
  • Dentinogenesis imperfecta (disorder)
  • Amelogenesis imperfecta - hypoplastic
  • Congenital enamel hypoplasia
  • Hyperplastic gingiva
  • Hyperplasia of gingiva
  • Hypocalcification of enamel of teeth
  • Dentinogenesis imperfecta with osteogenesis imperfecta
  • Amelogenesis imperfecta - hypomaturation - recessive pigmented
  • Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome
  • Osteogenesis imperfecta with opalescent teeth
  • Atypical dentin dysplasia due to SMOC2 deficiency
  • Horner teeth
  • Amelogenesis Imperfecta
  • Capdepont teeth
  • Pronounced occlusal groove
  • Amelogenesis imperfecta co-occurrent with cone rod dystrophy
  • Amelogenesis imperfecta (disorder)
  • Dentin dysplasia (disorder)
  • Amelogenesis imperfecta, hypoplastic type
  • Dentin dysplasia type 1 with microdontia and shape anomalies
  • Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta
  • Dentin dysplasia, sclerotic bones syndrome
  • Hypomineralisation of enamel of tooth
  • Microdontism
  • Hereditary opalescent dentine
  • Enamel-renal syndrome
  • Amelogenesis imperfecta, pigmented hypomaturation type
  • Shell teeth
  • Amelogenesis imperfecta - hypocalcified
  • Hypomineralisation of enamel of teeth
  • Dentinogenesis imperfecta - Shield's type II
  • Amelogenesis imperfecta and gingival hyperplasia syndrome
  • Amelogenesis imperfecta, hypocalcification type
  • Hypomineralisation of teeth
  • van de Hoeve syndrome
  • Trichodysplasia with amelogenesis imperfecta syndrome
  • Enamel hypomineralisation
  • Dentine dysplasia
  • Shell teeth (disorder)
  • Hereditary opalescent dentin
  • Hypocalcification of enamel of tooth
  • Rootless teeth
  • Platyspondyly amelogenesis imperfecta
  • Amelogenesis imperfecta - hypomaturation - autosomal dominant - hypoplastic with taurodontism
  • Verloes Bourguignon syndrome
  • Goldblatt syndrome
  • DGI
  • Amelogenesis imperfecta and nephrocalcinosis
  • Dentin dysplasia, type I
  • Dentine dysplasia - Shield's type I
  • Amelogenesis imperfecta - hypoplastic autosomal dominant - rough
  • Brachyolmia
  • Pulpal dysplasia
  • Dentin dysplasia with sclerotic bone syndrome
  • Odontochondrodysplasia
  • Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism
  • Taurodontism
  • Dentinogenesis imperfecta - Shield's type I
  • Amelogenesis imperfecta - hypomaturation
  • Jalili syndrome
  • Brandywine type of dentinogenesis imperfecta
  • Dentinogenesis imperfecta - Shield's type III
  • Deep occlusal groove
  • Amelogenesis imperfecta, hypoplastic type with microdontia
  • Dermo odontodysplasia
  • Dentine dysplasia - Shield's type II
  • Horner's teeth
  • Amelogenesis imperfecta - recessive - rough
  • Osteogenesis imperfecta type IB
  • Odontogenesis imperfecta (disorder)
  • Enamel hypomineralization
  • Hypomineralization of teeth
  • Dentin dysplasia, type II
  • Opalescent teeth with osteogenesis imperfecta
  • Amelogenesis imperfecta - hypoplastic autosomal dominant - local
  • Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome
  • Osteogenesis imperfecta type I
  • Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome
  • Hypomineralization of enamel of tooth
  • Dentin Dysplasias
  • McGibbon Lubinsky syndrome
  • Amelogenesis imperfecta - hypomineralization
  • Dysplasias, Dentin
  • Hypocalcification of enamel
  • AI - Amelogenesis imperfecta
  • Amelogenesis imperfecta - hypomineralisation
  • Congenital anomaly of sclera
Frequently Asked Questions
What is the ICD-10 code for hereditary disturbances in tooth structure, nec?

The ICD-10-CM code for hereditary disturbances in tooth structure, nec is K00.5. The full clinical description is "Hereditary disturbances in tooth structure, not elsewhere classified". K00.5 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code K00.5 mean?

ICD-10-CM code K00.5 represents “Hereditary disturbances in tooth structure, not elsewhere classified”. It is classified under Chapter 11: Diseases of the Digestive System and is a billable/specific code that can be used on a claim.

Is K00.5 a billable code?

Yes, K00.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is K00.5 in?

K00.5 is in Chapter 11: Diseases of the Digestive System (codes K00-K95).

What SNOMED CT codes does K00.5 map to?

K00.5 maps to 46 SNOMED CT concepts: 78494001, 109471001, 109475005, 109472008, 234965004, and 41 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for K00.5?

K00.5 is linked to 6 UMLS Concept Unique Identifiers: C0002452, C0011436, C0011430, C0868847, C0028878, and 1 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does K00.5 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary disturbances in tooth structure, nec 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 K00.5?

K00.5 maps to the ICD-11 code: LA30.Z (Structural developmental anomalies of teeth and periodontal tissues, 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.