Diagnosis Code: G11.4

Short Description: Hereditary spastic paraplegia

Long Description: Hereditary spastic paraplegia

The code G11.4 is VALID for claim submission

Code Classification:

• Diseases of the nervous system (G00–G99)
  • Systemic atrophies primarily affecting the central nervous system (G10-G14)
    • Hereditary ataxia (G11)
      • G11.4 Hereditary spastic paraplegia

Code Version: 2022 ICD-10-CM

Synonyms

• Autosomal dominant complex hereditary spastic paraplegia
• Autosomal dominant complex hereditary spastic paraplegia
• Autosomal dominant complex hereditary spastic paraplegia
• Autosomal dominant complex hereditary spastic paraplegia
• Autosomal dominant complex hereditary spastic paraplegia
• Autosomal dominant distal hereditary motor neuropathy
• Autosomal dominant hereditary spastic paraplegia
• Autosomal dominant spastic ataxia type 1
• Autosomal dominant spastic paraplegia type 10
• Autosomal dominant spastic paraplegia type 12
• Autosomal dominant spastic paraplegia type 13
• Autosomal dominant spastic paraplegia type 17
• Autosomal dominant spastic paraplegia type 19
• Autosomal dominant spastic paraplegia type 29
• Autosomal dominant spastic paraplegia type 3
• Autosomal dominant spastic paraplegia type 31
• Autosomal dominant spastic paraplegia type 36
• Autosomal dominant spastic paraplegia type 37
• Autosomal dominant spastic paraplegia type 38
• Autosomal dominant spastic paraplegia type 4
• Autosomal dominant spastic paraplegia type 41
• Autosomal dominant spastic paraplegia type 42
• Autosomal dominant spastic paraplegia type 6
• Autosomal dominant spastic paraplegia type 73
• Autosomal dominant spastic paraplegia type 8
• Autosomal dominant spastic paraplegia type 9A
• Autosomal dominant spastic paraplegia type 9B
• Autosomal recessive cerebellar ataxia with late-onset spasticity
• Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction
• Autosomal recessive hereditary spastic paraplegia
• Autosomal recessive spastic ataxia of Charlevoix-Saguenay
• Autosomal recessive spastic ataxia with leukoencephalopathy
• Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
• Autosomal recessive spastic paraplegia type 11
• Autosomal recessive spastic paraplegia type 14
• Autosomal recessive spastic paraplegia type 15
• Autosomal recessive spastic paraplegia type 18
• Autosomal recessive spastic paraplegia type 21
• Autosomal recessive spastic paraplegia type 23
• Autosomal recessive spastic paraplegia type 24
• Autosomal recessive spastic paraplegia type 25
• Autosomal recessive spastic paraplegia type 26
• Autosomal recessive spastic paraplegia type 27
• Autosomal recessive spastic paraplegia type 28
• Autosomal recessive spastic paraplegia type 32
• Autosomal recessive spastic paraplegia type 35
• Autosomal recessive spastic paraplegia type 39
• Autosomal recessive spastic paraplegia type 43
• Autosomal recessive spastic paraplegia type 44
• Autosomal recessive spastic paraplegia type 45
• Autosomal recessive spastic paraplegia type 46
• Autosomal recessive spastic paraplegia type 48
• Autosomal recessive spastic paraplegia type 53
• Autosomal recessive spastic paraplegia type 54
• Autosomal recessive spastic paraplegia type 55
• Autosomal recessive spastic paraplegia type 56
• Autosomal recessive spastic paraplegia type 57
• Autosomal recessive spastic paraplegia type 58
• Autosomal recessive spastic paraplegia type 59
• Autosomal recessive spastic paraplegia type 5A
• Autosomal recessive spastic paraplegia type 60
• Autosomal recessive spastic paraplegia type 61
• Autosomal recessive spastic paraplegia type 62
• Autosomal recessive spastic paraplegia type 63
• Autosomal recessive spastic paraplegia type 64
• Autosomal recessive spastic paraplegia type 66
• Autosomal recessive spastic paraplegia type 67
• Autosomal recessive spastic paraplegia type 69
• Autosomal recessive spastic paraplegia type 70
• Autosomal recessive spastic paraplegia type 71
• Autosomal recessive spastic paraplegia type 74
• Autosomal recessive spastic paraplegia type 75
• Autosomal recessive spastic paraplegia type 76
• Autosomal recessive spastic paraplegia type 77
• Autosomal recessive spastic paraplegia type 78
• Autosomal recessive spastic paraplegia type 9B
• Autosomal spastic paraplegia type 30
• Autosomal spastic paraplegia type 72
• Bedouin spastic ataxia syndrome
• Bilateral lower limb ataxia
• Choreoathetosis
• Chronic deafness
• Complicated hereditary spastic paraplegia
• Congenital miosis
• Constricted pupil
• Disorder of glutamine metabolism
• Distal spinal muscular atrophy
• Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome
• Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome
• Fryns macrocephaly
• Hereditary sensory and autonomic neuropathy with spastic paraplegia
• Hereditary spastic paraplegia
• Infantile ascending hereditary spastic paralysis
• Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome
• Macular corneal dystrophy
• Maternally inherited mitochondrial deoxyribonucleic acid disease
• Motor neuron disease due to hereditary spastic paraplegia
• MT-ATP6-related mitochondrial spastic paraplegia
• Palmoplantar keratoderma, spastic paralysis syndrome
• Parkinsonism due to hereditary spastic paraplegia
• Parkinsonism due to heredodegenerative disorder
• Paroxysmal choreoathetosis
• Paroxysmal dystonia
• Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity
• Progressive muscular atrophy
• Punctate palmoplantar keratoderma
• Pure hereditary spastic paraplegia
• Second cranial nerve finding
• Second cranial nerve finding
• Second cranial nerve finding
• Second cranial nerve finding
• Second cranial nerve finding
• Second cranial nerve finding
• Second cranial nerve finding
• Severe intellectual disability and progressive spastic paraplegia
• Spastic ataxia with congenital miosis
• Spastic ataxia, dysarthria due to glutaminase deficiency
• Spastic paraparesis
• Spastic paraparesis and deafness
• Spastic paraplegia type 7
• Spastic paraplegia with Paget disease of bone syndrome
• Spastic paraplegia with precocious puberty syndrome
• Spastic paraplegia, facial cutaneous lesion syndrome
• Spastic paraplegia, glaucoma, intellectual disability syndrome
• Spastic paraplegia, nephritis, deafness syndrome
• Spastic paraplegia, neuropathy, poikiloderma syndrome
• Spastic paraplegia, optic atrophy, neuropathy syndrome
• Spastic paraplegia, severe developmental delay, epilepsy syndrome
• SPOAN and SPOAN-related disorder
• SPOAN and SPOAN-related disorder
• SPOAN and SPOAN-related disorder
• SPOAN and SPOAN-related disorder
• SPOAN and SPOAN-related disorder
• X-linked complex hereditary spastic paraplegia
• X-linked hereditary spastic paraplegia
• X-linked pure hereditary spastic paraplegia
• X-linked spastic paraplegia type 16
• X-linked spastic paraplegia type 2
• X-linked spastic paraplegia type 34

Crosswalk Information

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

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