G11.4
BillableHereditary spastic paraplegia
Hereditary spastic paraplegia
Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- cerebral palsy (G80.-)
- hereditary and idiopathic neuropathy (G60.-)
- metabolic disorders (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Familial spastic paraplegia syndrome39912006
- HSP - Hereditary spastic paraplegia39912006
- Hereditary spastic paraplegia39912006
- Spastic congenital paraplegia39912006
- Strumpell-Lorrain disease39912006
- Choreoathetosis43105007
- Paroxysmal choreoathetosis49949003
- Paroxysmal dyskinesia49949003
- Macular corneal dystrophy60258001
- Duchenne-Aran muscular atrophy88923002
- PMA - Progressive muscular atrophy88923002
- Progressive muscular atrophy88923002
- Pure progressive muscular atrophy88923002
- Optic nerve finding106152006
- Second cranial nerve finding106152006
- Disorder of glutamine metabolism190724004
- Disturbance of glutamine metabolism190724004
- Distal spinal muscular atrophy230247001
- Pure hereditary spastic paraplegia230260007
- Complicated hereditary spastic paraplegia230261006
- Autosomal dominant spastic paraplegia type 17230263009
- Silver disease230263009
- Paroxysmal dystonia230310003
- Chronic deafness232325008
- Miotic pupil301939004
- Constricted pupil301939004
- Miosis301939004
- Pupil constriction301939004
- Small pupil301939004
- Spastic paraparesis312444006
- Congenital miosis400962005
- Punctate palmoplantar keratoderma402773000
- ARSACS - autosomal recessive spastic ataxia of Charlevoix-Saguenay702445005
- Autosomal recessive spastic ataxia of Charlevoix-Saguenay702445005
- Spastic ataxia of Charlevoix-Saguenay702445005
- IAHSP - infantile onset ascending hereditary spastic paralysis703543005
- Infantile ascending hereditary spastic paralysis703543005
- Infantile-onset ascending hereditary spastic paralysis703543005
- Bedouin spastic ataxia syndrome715465001
- Mousa-Al Din-Al Nassar syndrome715465001
- Spastic ataxia and corneal dystrophy715465001
- Spinocerebellar degeneration co-occurrent with macular corneal dystrophy715465001
- Autosomal recessive spastic paraplegia type 11715491000
- Nakamura Osame syndrome715491000
- Spastic paraplegia, intellectual disability and thin corpus callosum715491000
- Spastic paraparesis and deafness715504003
- Spastic paraparesis co-occurrent with deafness715504003
- Wells Jankovic syndrome715504003
- Dystonia 9715564000
- Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity715564000
- Spastic paraplegia type 7715776003
- Fryns macrocephaly716108004
- Macrocephaly with spastic paraplegia and dysmorphism syndrome716108004
- HSAN (hereditary sensory and autonomic neuropathy) with spastic paraplegia717827000
- Hereditary sensory and autonomic neuropathy with spastic paraplegia717827000
- Autosomal recessive spastic paraplegia type 39719103009
- Spastic paraplegia due to NTE (neuropathy target esterase) mutation719103009
- Spastic paraplegia due to neuropathy target esterase mutation719103009
- Parkinsonism due to hereditary spastic paraplegia722599008
- Parkinsonism due to heredodegenerative disorder722965000
- Spastic gait type 2723622007
- Spastic paraparesis type 2723622007
- Spastic paraplegia type 2723622007
- X-linked spastic paraplegia type 2723622007
- Autosomal dominant spastic paraplegia type 36723819007
- Autosomal dominant spastic paraplegia type 4723820001
- Autosomal recessive spastic paraplegia type 44723821002
- Autosomal recessive spastic paraplegia type 46723822009
- Autosomal recessive spastic paraplegia type 53723823004
- Autosomal recessive spastic paraplegia type 54723824005
- Autosomal recessive spastic paraplegia type 55723825006
- Autosomal recessive spastic paraplegia type 57723826007
- Spastic paraplegia due to partial TFG deficiency723826007
- X-linked hereditary spastic paraplegia724775006
- SPOAN (spastic paraplegia, optic atrophy, neuropathy) syndrome725139005
- Spastic paraplegia, optic atrophy, neuropathy syndrome725139005
- Autosomal recessive spastic paraplegia type 32726606003
- Autosomal recessive spastic paraplegia type 26726607007
- GM2 synthase deficiency726607007
- Autosomal recessive spastic paraplegia type 23726608002
- Lison syndrome726608002
- Spastic paraparesis, vitiligo, premature graying, characteristic facies syndrome726608002
- Spastic paraparesis, vitiligo, premature greying, characteristic facies syndrome726608002
- Autosomal recessive spastic paraplegia type 64726609005
- Autosomal recessive spastic paraplegia type 63726610000
- Autosomal recessive spastic paraplegia type 61726611001
- Spastic paraplegia with Paget disease of bone syndrome726622002
- Autosomal recessive spastic paraplegia type 18732932004
- Autosomal recessive spastic paraplegia disc herniation syndrome732933009
- Autosomal recessive spastic paraplegia type 25732933009
- Autosomal dominant spastic paraplegia type 10732948003
- Autosomal dominant familial spastic paraplegia type 3732949006
- Autosomal dominant spastic paraplegia type 6732949006
- Spastic paraplegia with precocious puberty syndrome732958004
- Autosomal dominant spastic paraplegia type 29733029008
- Fitzsimmons Walson Mellor syndrome733089005
- Spastic paraplegia, nephritis, deafness syndrome733089005
- Spastic paraplegia, glaucoma, intellectual disability syndrome733455003
- Autosomal dominant hereditary spastic paraplegia737227004
- Autosomal dominant spastic paraplegia type 31763068005
- Autosomal dominant spastic paraplegia type 41763069002
- Autosomal dominant spastic paraplegia type 42763070001
- Autosomal recessive cerebellar ataxia due to GBA2 (glucosylceramidase beta 2) deficiency763348005
- Autosomal recessive cerebellar ataxia with late-onset spasticity763348005
- Autosomal recessive spastic paraplegia type 48763367009
- Autosomal dominant spastic paraplegia type 37763369007
- X-linked spastic paraplegia type 34763370008
- Autosomal recessive spastic paraplegia type 5A763373005
- Autosomal dominant spastic paraplegia type 12763374004
- Autosomal dominant spastic paraplegia type 19763375003
- Autosomal recessive spastic paraplegia type 28763376002
- Autosomal spastic paraplegia type 30763377006
- Antinolo Nieto Borrego syndrome763402002
- Spastic paraplegia, neuropathy, poikiloderma syndrome763402002
- Bahemuka Brown syndrome763403007
- Spastic paraplegia, facial cutaneous lesion syndrome763403007
- Autosomal dominant spastic ataxia type 7763669001
- Spastic ataxia with congenital miosis763669001
- Autosomal recessive spastic paraplegia type 15764686003
- Hereditary spastic paraparesis type 15764686003
- Kjellin syndrome764686003
- Spastic paraplegia, retinal degeneration syndrome764686003
- Autosomal recessive spastic paraplegia type 35764688002
- Autosomal recessive spastic paraplegia type 21764734003
- Mast syndrome764734003
- Autosomal recessive spastic paraplegia type 43764736001
- Autosomal recessive spastic paraplegia type 62765045003
- Autosomal recessive spastic paraplegia type 45765753004
- Autosomal recessive spastic paraplegia type 67766767001
- Autosomal recessive spastic ataxia type 2770720005
- Autosomal recessive spastic paraplegia type 58770720005
- Autosomal recessive spastic paraplegia type 70770724001
- AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome771469002
- AFG3L2-related spastic ataxia, myoclonic epilepsy, neuropathy syndrome771469002
- Autosomal recessive spastic ataxia type 5771469002
- Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome771469002
- Autosomal recessive spastic paraplegia type 59773425000
- AP4 deficiency syndrome778011005
- Severe intellectual disability and progressive spastic paraplegia778011005
- Autosomal recessive spastic paraplegia type 27778030005
- MT-ATP6-related mitochondrial spastic paraplegia778048001
- Maternally-inherited spastic paraplegia778048001
- Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia778048001
- Autosomal dominant spastic paraplegia type 3782670003
- Strumpell disease782670003
- Autosomal recessive spastic paraplegia type 69782725000
- Autosomal recessive spastic paraplegia type 71782726004
- Autosomal spastic paraplegia type 72782727008
- Autosomal recessive spastic paraplegia type 60782746009
- Autosomal recessive spastic paraplegia type 66782747000
- Autosomal recessive spastic paraplegia type 14783094006
- Autosomal dominant spastic paraplegia type 38783622001
- X-linked spastic paraplegia type 16783697000
- Autosomal dominant spastic paraplegia type 13783698005
- Autosomal recessive spastic paraplegia type 56783764008
- ARSAL - autosomal recessive spastic ataxia with leucoencephalopathy784343003
- ARSAL - autosomal recessive spastic ataxia with leukoencephalopathy784343003
- Autosomal recessive spastic ataxia type 3784343003
- Autosomal recessive spastic ataxia with leucoencephalopathy784343003
- Autosomal recessive spastic ataxia with leukoencephalopathy784343003
- SPAX3 - autosomal recessive spastic ataxia type 3784343003
- Autosomal recessive spastic ataxia type 4784347002
- Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome784347002
- SPAX 4 - autosomal recessive spastic ataxia type 4784347002
- Autosomal dominant spastic ataxia type 1784380009
- SPAX1 - autosomal dominant spastic ataxia type 1784380009
- Autosomal recessive spastic paraplegia type 24785304005
- Autosomal dominant spastic paraplegia type 8785305006
- Palmoplantar keratoderma, spastic paralysis syndrome785725008
- Powell Venencie Gordon syndrome785725008
- SPOAN and SPOAN-related disorder789674008
- Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder789674008
- Ataxia of bilateral lower extremities830119000
- Ataxia of bilateral lower limbs830119000
- Ataxia of both lower limbs830119000
- Ataxia of left and right lower limbs830119000
- Bilateral lower limb ataxia830119000
- Autosomal dominant distal hereditary motor neuropathy1156837002
- X-linked complex hereditary spastic paraplegia1156841003
- X-linked pure hereditary spastic paraplegia1156842005
- Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome1172588008
- Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome1172590009
- Autosomal recessive spastic paraplegia type 761172631001
- Autosomal recessive spastic paraplegia type 781177168007
- SPG78 - autosomal recessive spastic paraplegia type 781177168007
- Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction1186734006
- Autosomal recessive spastic paraplegia type 741187191003
- SPPRS (spastic paraplegia, psychomotor retardation, seizures) syndrome1187278006
- Spastic paraplegia, severe developmental delay, epilepsy syndrome1187278006
- Autosomal recessive hereditary spastic paraplegia1187279003
- Autosomal dominant spastic paraplegia type 9A1187465008
- Cataracts, motor neuropathy, short stature, skeletal anomalies syndrome1187465008
- Spastic paraparesis, amyotrophy, cataracts, gastro-oesophageal reflux syndrome1187465008
- Spastic paraparesis, amyotrophy, cataracts, gastroesophageal reflux syndrome1187465008
- Autosomal dominant spastic paraplegia type 9B1187466009
- Autosomal recessive spastic paraplegia type 9B1187467000
- Autosomal dominant spastic paraplegia type 731187468005
- Autosomal recessive spastic paraplegia type 751187470001
- Autosomal recessive spastic paraplegia type 771187506008
- Spastic ataxia, dysarthria due to glutaminase deficiency1255323007
- Autosomal dominant complex hereditary spastic paraplegia1259038005
- SINO syndrome1260134001
- Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome1260134001
- Dystonia due to hereditary spastic paraplegia1260397000
- Motor neuron disease due to hereditary spastic paraplegia1263536006
- Fatty acyl-CoA reductase 1 superactivity1360070001
- Spastic paraparesis, cataracts, speech delay syndrome1360070001
- MT-ATP6 mitochondrial disease1363509005
- Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial disease1363509005
UMLS
- Familial spastic paraplegia syndromeC0037773
- HSP - Hereditary spastic paraplegiaC0037773
- Hereditary Spastic ParaplegiaC0037773
- Hereditary Spastic ParaplegiasC0037773
- Hereditary spastic paraplegiaC0037773
- Hereditary spastic paraplegia (disorder)C0037773
- Hypertrophic Motor Sensory Neuropathy Spastic ParaplegiaC0037773
- Hypertrophic Motor-Sensory Neuropathy-Spastic ParaplegiaC0037773
- Paraplegia, Hereditary SpasticC0037773
- Paraplegia, Spastic, HereditaryC0037773
- Paraplegias, Hereditary SpasticC0037773
- Spastic Paraplegia Hypertrophic Motor Sensory NeuropathyC0037773
- Spastic Paraplegia, HereditaryC0037773
- Spastic Paraplegia-Hypertrophic Motor-Sensory NeuropathyC0037773
- Spastic Paraplegias, HereditaryC0037773
- Spastic congenital paraplegiaC0037773
- Strumpell-Lorrain diseaseC0037773
- hereditary spastic paraplegiaC0037773
- hereditary spastic paraplegiasC0037773
- spastic paraplegia hereditaryC0037773
Frequently Asked Questions
What is the ICD-10 code for hereditary spastic paraplegia?
The ICD-10-CM code for hereditary spastic paraplegia is G11.4. The full clinical description is "Hereditary spastic paraplegia". G11.4 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G11.4 mean?
ICD-10-CM code G11.4 represents "Hereditary spastic paraplegia". It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.
Is G11.4 a billable code?
Yes, G11.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G11.4 in?
G11.4 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G11.4 map to?
G11.4 maps to 128 SNOMED CT concepts: 301939004, 771469002, 778011005, 702445005, 784343003, and 123 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G11.4?
G11.4 is linked to 1 UMLS Concept Unique Identifier: C0037773. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.