G11.5
BillableHypomyelination - hypogonadotropic hypogonadism - hypodontia
Hypomyelination - hypogonadotropic hypogonadism - hypodontia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- 4H syndrome
- Pol III-related leukodystrophy
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
UMLS
- 4H LEUKODYSTROPHY 1C2676243
- 4H SYNDROMEC2676243
- 4H syndromeC2676243
- ADDHC2676243
- ATAXIA, DELAYED DENTITION, AND HYPOMYELINATIONC2676243
- Ataxia, Delayed Dentition, and HypomyelinationC2676243
- Ataxia, delayed dentition, and hypomyelinationC2676243
- HLD7C2676243
- Hypomyelinating Leukodystrophy-7C2676243
- Hypomyelination - hypogonadotropic hypogonadism - hypodontiaC2676243
- Hypomyelination, hypodontia, hypogonadotropic hypogonadismC2676243
- Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndromeC2676243
- Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder)C2676243
- LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISMC2676243
- LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPIC HYPOGONADISMC2676243
- LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITIONC2676243
- Leukodystrophy, Hypomyelinating, 7C2676243
- Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic HypogonadismC2676243
- Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadismC2676243
- Leukoencephalopathy, Hypomyelinating, with Ataxia and Delayed DentitionC2676243
- Leukoencephalopathy-ataxia-hypodontia-hypomyelinationC2676243
- Pol III disorderC4038750
- Pol III-related hypomyelinating leukodystrophiesC4038750
- Pol III-related leukodystrophyC4038750
- RNA polymerase III-related leucodystrophyC4038750
- RNA polymerase III-related leukodystrophyC4038750
- Ribonucleic acid polymerase III-related leucodystrophyC4038750
- Ribonucleic acid polymerase III-related leukodystrophyC4038750
- Ribonucleic acid polymerase III-related leukodystrophy (disorder)C4038750
Frequently Asked Questions
What is ICD-10 code G11.5?
ICD-10-CM code G11.5 represents "Hypomyelination - hypogonadotropic hypogonadism - hypodontia". It is a billable/specific code that can be used on a claim.
Is G11.5 a billable code?
Yes, G11.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G11.5 in?
G11.5 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G11.5 map to?
G11.5 maps to 2 SNOMED CT concepts: 1208933000, 721846006. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G11.5?
G11.5 is linked to 2 UMLS Concept Unique Identifiers: C2676243, C4038750. 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.