ORPHA:522580

Secondary early-onset glaucoma of genetic origin

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	Secondary early-onset glaucoma of genetic origin
fr	Glaucome à début précoce secondaire d'origine génétique
de	Genetisch bedingtes Sekundärglaukom mit frühem Beginn
es	Glaucoma secundario de inicio precoz de origen genético
it	Glaucoma secondario a esordio precoce di origine genetica
nl	Secundair vroeg optredend glaucoom van genetische oorsprong
pt	Glaucoma secundário de início precoce com origem genética
pl	Wtórna jaskra o wczesnym początku uwarunkowana genetycznie
cs	Geneticky podmíněný sekundární glaukom s časným nástupem
uk	Генетично обумовлена вторинна рання глаукома
zh	遗传继发性早发型青光眼
tr	Genetik kökenli sekonder erken başlangıçlı glokom

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C5681404	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 (1):

ORPHA:359Pediatric-onset glaucoma of genetic origin
rare genetic diseases

Children (2):

Codes that Orphanet moved or referred to this one:

ORPHA:98637OBSOLETE: Secondary glaucoma due to a proliferation and differentiation anomaly 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/522580
This record as JSON: /data/d/522580.json