Kodex

Code

G11.5

Hypomyelination - hypogonadotropic hypogonadism - hypodontia

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Hierarchy

G00-G99 Diseases of the nervous system (G00-G99)
- G10-G14 Systemic atrophies primarily affecting the central nervous system (G10-G14)
  - G11 Hereditary ataxia
    - G11.0 Congenital nonprogressive ataxia
    - G11.1 Early-onset cerebellar ataxia
    - G11.2 Late-onset cerebellar ataxia
    - G11.3 Cerebellar ataxia with defective DNA repair
    - G11.4 Hereditary spastic paraplegia
    - G11.5 Hypomyelination - hypogonadotropic hypogonadism - hypodontia
    - G11.6 Leukodystrophy with vanishing white matter disease
    - G11.8 Other hereditary ataxias
    - G11.9 Hereditary ataxia, unspecified

Inclusion Terms

G11.5

4H syndrome
Pol III-related leukodystrophy

Excludes 2

G80 Cerebral palsy
G60 Hereditary and idiopathic neuropathy
E70-E88 Metabolic disorders (E70-E88)

certain conditions originating in the perinatal period (P04-P96)
A00-B99 Certain infectious and parasitic diseases (A00-B99)
complications of pregnancy, childbirth and the puerperium (O00-O9A)
- O00-O9A Pregnancy, childbirth and the puerperium (O00-O9A)
congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
endocrine, nutritional and metabolic diseases (E00-E88)
S00-T88 Injury, poisoning and certain other consequences of external causes (S00-T88)
C00-D49 Neoplasms (C00-D49)
symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)