ORPHA:98671

Hereditary optic neuropathy

Type: Category
Group: Group of disorders
Status: active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Hereditary optic neuropathy
fr	Neuropathie optique héréditaire
de	Optikus-Neuropathie, hereditäre
es	Neuropatía óptica hereditaria
it	Neuropatia ottica ereditaria
nl	Hereditaire opticusneuropathie	Erfelijke optische neuropathie
pt	Neuropatia óptica hereditária
pl	Dziedziczna neuropatia nerwu wzrokowego
cs	Hereditární optické neuropatie
uk	Спадкова нейропатія зорового нерва
zh	遗传性视神经病变
tr	Kalıtsal optik nöropati

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-11	9C40.8	E	specific	validated
MONDO	0020249	E		validated
MedDRA	10061323	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:97966Rare ophthalmic disorder

Parents in the classifications (2):

ORPHA:522512Rare genetic optic nerve disorder
rare genetic diseases
ORPHA:519351Rare optic nerve disorder
rare ophthalmic disorders

Children (5):

Codes that Orphanet moved or referred to this one:

ORPHA:103OBSOLETE: Genetic optic atrophy referred to · inactive
ORPHA:98675OBSOLETE: Autosomal recessive optic atrophy referred to · inactive
ORPHA:98678OBSOLETE: X-linked recessive optic atrophy referred to · inactive

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/98671
This record as JSON: /data/d/98671.json