Diagnosis Code: K00.5

Short Description: Hereditary disturbances in tooth structure, NEC

Long Description: Hereditary disturbances in tooth structure, not elsewhere classified

The code K00.5 is VALID for claim submission

Code Classification:

• Diseases of the digestive system (K00–K95)
  • Diseases of oral cavity and salivary glands (K00-K14)
    • Disorders of tooth development and eruption (K00)
      • K00.5 Hereditary disturbances in tooth structure, NEC

Code Version: 2022 ICD-10-CM

Synonyms

• Amelogenesis imperfecta
• Amelogenesis imperfecta - hypomaturation - recessive pigmented
• Amelogenesis imperfecta - hypomaturation - snow capped teeth
• Amelogenesis imperfecta - hypoplastic autosomal dominant - local
• Amelogenesis imperfecta - hypoplastic autosomal dominant - rough
• Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth
• Amelogenesis imperfecta - recessive - rough
• Amelogenesis imperfecta and gingival hyperplasia syndrome
• Amelogenesis imperfecta co-occurrent with cone rod dystrophy
• Amelogenesis imperfecta, hypocalcification type
• Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism
• Amelogenesis imperfecta, hypomaturation type
• Amelogenesis imperfecta, hypomaturation type
• Amelogenesis imperfecta, hypoplastic type
• Amelogenesis imperfecta, hypoplastic type
• Amelogenesis imperfecta, hypoplastic type
• Amelogenesis imperfecta, hypoplastic type with microdontia
• Amelogenesis imperfecta, pigmented hypomaturation type
• Atypical dentin dysplasia due to SMOC2 deficiency
• Brachyolmia
• Congenital anomaly of sclera
• Deep occlusal groove
• Dentin dysplasia
• Dentin dysplasia
• Dentin dysplasia with sclerotic bone syndrome
• Dentin dysplasia, type I
• Dentin dysplasia, type II
• Dentinogenesis imperfecta
• Dentinogenesis imperfecta
• Dentinogenesis imperfecta
• Dentinogenesis imperfecta
• Dentinogenesis imperfecta
• Dentinogenesis imperfecta - Shield's type I
• Dentinogenesis imperfecta - Shield's type II
• Dentinogenesis imperfecta - Shield's type III
• Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
• Dermo-odonto dysplasia
• Enamel-renal syndrome
• Goldblatt syndrome
• Horner's teeth
• Hyperplasia of gingiva
• Hypocalcification of teeth
• Hypomineralization of enamel of teeth
• Hypomineralization of enamel of tooth
• Hypomineralization of tooth
• Microdontia
• Nephrocalcinosis
• Odontogenesis imperfecta
• Osteogenesis imperfecta type I
• Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta
• Osteosclerosis
• Shell teeth
• Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome
• Taurodontism
• Trichodysplasia with amelogenesis imperfecta syndrome
• Verloes Bourguignon syndrome

References to Index of Diseases and Injuries

The code K00.5 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Amelogenesis imperfecta
  • Dentinogenesis imperfecta
  • Odontogenesis imperfecta
  • Dentinal dysplasia
  • Shell teeth

Crosswalk Information

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This page was last updated on: 10/1/2023

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