K00.5
BillableHereditary disturbances in tooth structure, NEC
Hereditary disturbances in tooth structure, not elsewhere classified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Amelogenesis imperfecta
- Dentinogenesis imperfecta
- Odontogenesis imperfecta
- Dentinal dysplasia
- Shell teeth
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •embedded and impacted teethK01
Related Codes(9)
K00.0Anodontia
K00.1Supernumerary teeth
K00.2Abnormalities of size and form of teeth
K00.3Mottled teeth
K00.4Disturbances in tooth formation
K00.6Disturbances in tooth eruption
K00.7Teething syndrome
K00.8Other disorders of tooth development
K00.9Disorder of tooth development, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(247)
SNOMED CT
- Hypocalcification of teeth26748006
- Hypomineralisation of teeth26748006
- Hypomineralization of teeth26748006
- Microdontia32337007
- Microdontism32337007
- Congenital abnormality of sclera32809005
- Congenital anomaly of sclera32809005
- Osteosclerosis49347007
- Taurodontism51744007
- Osteogenesis imperfecta type IB63890001
- Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta63890001
- Osteogenesis imperfecta with opalescent teeth63890001
- Shell teeth67504007
- AI - Amelogenesis imperfecta78494001
- Amelogenesis imperfecta78494001
- Congenital enamel hypoplasia78494001
- Amelogenesis imperfecta - hypocalcified109471001
- Amelogenesis imperfecta - hypomineralisation109471001
- Amelogenesis imperfecta - hypomineralization109471001
- Amelogenesis imperfecta, hypocalcification type109471001
- Amelogenesis imperfecta - hypomaturation - autosomal dominant - hypoplastic with taurodontism109472008
- Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism109472008
- Amelogenesis imperfecta, hypoplastic type with microdontia109473003
- Amelogenesis imperfecta, pigmented hypomaturation type109474009
- Amelogenesis imperfecta - hypomaturation109475005
- Amelogenesis imperfecta, hypomaturation type109475005
- Amelogenesis imperfecta - hypoplastic109476006
- Amelogenesis imperfecta, hypoplastic type109476006
- Amelogenesis imperfecta and nephrocalcinosis109477002
- Amelogenesis imperfecta, nephrocalcinosis and impaired renal concentration109477002
- Enamel renal syndrome109477002
- Enamel-renal syndrome109477002
- McGibbon Lubinsky syndrome109477002
- Enamel hypomineralisation109487003
- Enamel hypomineralization109487003
- Hypocalcification of enamel109487003
- Hypocalcification of enamel of tooth109487003
- Hypomineralisation of enamel of tooth109487003
- Hypomineralization of enamel of tooth109487003
- Dentin dysplasia109492001
- Dentinal dysplasia109492001
- Dentine dysplasia109492001
- Dentin dysplasia, type I109493006
- Dentine dysplasia - Shield's type I109493006
- Radicular dentine dysplasia109493006
- Rootless teeth109493006
- Anomalous dysplasia of dentine109494000
- Coronal dentine dysplasia109494000
- Dentin dysplasia, type II109494000
- Dentine dysplasia - Shield's type II109494000
- Pulpal dysplasia109494000
- Horner teeth111325003
- Horner's teeth111325003
- Dentinogenesis imperfecta196286005
- Hereditary opalescent dentin196286005
- Odontogenesis imperfecta196287001
- Amelogenesis imperfecta - hypoplastic autosomal dominant - local234961008
- Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth234962001
- Amelogenesis imperfecta - hypoplastic autosomal dominant - rough234963006
- Amelogenesis imperfecta - recessive - rough234964000
- Amelogenesis imperfecta - hypomaturation - recessive pigmented234965004
- Amelogenesis imperfecta - hypomaturation - snow capped teeth234966003
- Dentinogenesis imperfecta - Shield's type I234968002
- Dentinogenesis imperfecta with osteogenesis imperfecta234968002
- Opalescent teeth with osteogenesis imperfecta234968002
- Capdepont teeth234969005
- Dentinogenesis imperfecta - Shield's type II234969005
- Dentinogenesis imperfecta without osteogenesis imperfecta234969005
- Hereditary opalescent dentine234969005
- Brandywine type of dentinogenesis imperfecta234970006
- Dentinogenesis imperfecta - Shield's type III234970006
- Brachyolmia254088006
- Osteogenesis imperfecta type I385482004
- van de Hoeve syndrome385482004
- Hyperplasia of gingiva441798003
- Hyperplastic gingiva441798003
- Deep occlusal groove699685006
- Pronounced occlusal groove699685006
- Amelogenesis imperfecta and gingival hyperplasia syndrome707607008
- Amelogenesis imperfecta co-occurrent with cone rod dystrophy707608003
- Jalili syndrome707608003
- Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome716195006
- Brachyolmia and amelogenesis imperfecta syndrome716195006
- Platyspondyly amelogenesis imperfecta716195006
- Verloes Bourguignon syndrome716195006
- Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome717823001
- Goldblatt chondrodysplasia717823001
- Goldblatt syndrome717823001
- Odontochondrodysplasia717823001
- Trichodysplasia with amelogenesis imperfecta syndrome719911000
- Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome721089006
- Dermo odontodysplasia721091003
- Dermo-odonto dysplasia721091003
- Dermoodonto dysplasia721091003
- Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome733468006
- Suarez Stickler syndrome733468006
- Dentin dysplasia with sclerotic bone syndrome770943008
- Dentin dysplasia, sclerotic bones syndrome770943008
- Atypical dentin dysplasia due to SMOC2 deficiency783059004
- Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency783059004
- Dentin dysplasia type 1 with microdontia and shape anomalies783059004
- Hypocalcification of enamel of teeth1258915002
- Hypomineralisation of enamel of teeth1258915002
- Hypomineralization of enamel of teeth1258915002
UMLS
- AI - Amelogenesis imperfectaC0002452
- Amelogenesis ImperfectaC0002452
- Amelogenesis imperfectaC0002452
- Amelogenesis imperfecta (disorder)C0002452
- Congenital Enamel HypoplasiaC0002452
- Congenital enamel hypoplasiaC0002452
- amelogenesis imperfectaC0002452
- DGIC0011436
- Dentinogenesis ImperfectaC0011436
- Dentinogenesis imperfectaC0011436
- Dentinogenesis imperfecta (disorder)C0011436
- Hereditary opalescent dentinC0011436
- dentinogenesis imperfectaC0011436
- Dentin DysplasiaC0011430
- Dentin DysplasiasC0011430
- Dentin dysplasiaC0011430
- Dentin dysplasia (disorder)C0011430
- Dentinal dysplasiaC0011430
- Dentine dysplasiaC0011430
- Dysplasia, DentinC0011430
- Dysplasias, DentinC0011430
- dentin dysplasiaC0011430
- dentinal dysplasiaC0011430
- Hereditary disturbances in tooth structure, NECC0868847
- Hereditary disturbances in tooth structure, not elsewhere classifiedC0868847
- Odontogenesis ImperfectaC0028878
- Odontogenesis imperfectaC0028878
- Odontogenesis imperfecta (disorder)C0028878
- Shell teethC2981132
- Shell teeth (disorder)C2981132
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.