Diagnosis Code: F79

Short Description: Unspecified intellectual disabilities

Long Description: Unspecified intellectual disabilities

The code F79 is VALID for claim submission

Code Classification:

• Mental and behavioural disorders (F01–F99)
  • Intellectual disabilities (F70-F79)
    • Unspecified intellectual disabilities (F79)
      • F79 Unspecified intellectual disabilities

Code Version: 2022 ICD-10-CM

Synonyms

• 11p partial monosomy syndrome
• ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder
• Arachnodactyly
• Arachnodactyly
• Arachnodactyly and intellectual disability with facial dysmorphism syndrome
• Arachnodactyly with abnormal ossification and intellectual disability syndrome
• Athetoid cerebral palsy
• Below average intellect
• Blepharophimosis, intellectual disability syndrome
• Blepharophimosis, intellectual disability syndrome
• Brachycephaly
• Brachydactyly, mesomelia, intellectual disability, heart defect syndrome
• Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome
• Childhood obesity
• Combined malformation of central nervous system and skeletal muscle
• Congenital blepharophimosis
• Congenital blepharophimosis
• Congenital hepatic fibrosis
• Congenital nuclear ophthalmoplegia
• Congenital plicated tongue
• Cryptorchidism, arachnodactyly, intellectual disability syndrome
• Deletion of part of chromosome 11
• Deletion of part of chromosome 21
• Disorder of sex development with intellectual disability syndrome
• DYRK1A-related intellectual disability syndrome
• DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
• Dyskinetic cerebral palsy
• Hepatic fibrosis, renal cyst, intellectual disability syndrome
• Hypertelorism
• Hypogonadism with mitral valve prolapse and intellectual disability syndrome
• Intellectual disability
• Intellectual disability due to nutritional deficiency
• Intellectual disability Wolff type
• Intellectual disability, brachydactyly, Pierre Robin syndrome
• Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
• Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome
• Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome
• Intellectual disability, polydactyly, uncombable hair syndrome
• Intellectual disability, seizures, macrocephaly, obesity syndrome
• Intellectual disability, severe speech delay, mild dysmorphism syndrome
• Intellectual disability, short stature, hypertelorism syndrome
• Intellectual functioning disability
• Kagami Ogata syndrome
• Low intelligence
• Mesomelic dysplasia of upper limb
• Microcephaly, seizure, intellectual disability, heart disease syndrome
• Micromelia
• Non-spastic cerebral palsy
• Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome
• Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome
• Paralysis of tongue
• Pervasive developmental disorder with disorder of intellectual development with loss of previously acquired skills
• Pervasive developmental disorder with disorder of intellectual development without loss of previously acquired skills
• Plicated tongue
• Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome
• PPP2R5D-related intellectual disability
• Premature ovarian failure
• Robin sequence
• Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome
• WAGR syndrome
• White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome
• White Sutton syndrome

References to Index of Diseases and Injuries

The code F79 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Mental deficiency NOS
  • Mental subnormality NOS

Crosswalk Information

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

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