ORPHA:98634
Anterior segment developmental anomaly without extraocular manifestations
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Anterior segment developmental anomaly without extraocular manifestations | |
| fr | Anomalie du développement du segment antérieur de l'oeil sans manifestations extra-oculaires | |
| de | Anomalie des vorderen Augensegmentes ohne extraokuläre Manifestationen | |
| es | Anomalía del desarrollo del segmento anterior sin manifestaciones extraoculares | |
| it | Iridogoniodisgenesia | |
| nl | Ontwikkelingsanomalie van voorste oogsegment zonder extraoculaire manifestaties | |
| pt | Iridogoniodisgenesia | |
| pl | Irydogoniodysgeneza | |
| cs | Iridogoniodysgeneze | |
| uk | Аномалія розвитку переднього сегмента без екстраочних проявів | |
| zh | 无眼外表现眼球前区发育异常 | |
| tr | Ekstraoküler belirtileri olmayan anterior segment gelişimsel anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 11119 | E | validated | |
| UMLS | C5681672 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (4):
- ORPHA:88632Anterior segment developmental anomaly
rare developmental anomalies during embryogenesis; rare ophthalmic disorders - ORPHA:522540Anterior segment developmental anomaly of genetic origin
rare genetic diseases - ORPHA:98631Congenital malformation of the eye with glaucoma as a major feature
rare developmental anomalies during embryogenesis; rare ophthalmic disorders - ORPHA:525677Genetic congenital malformation of the eye with glaucoma as a major feature
rare genetic diseases
Children (11):
- ORPHA:519388Autosomal recessive anterior segment dysgenesis
- ORPHA:98978Axenfeld anomaly
- ORPHA:69736Bilateral acute depigmentation of the iris
- ORPHA:98944Coloboma of iris
- ORPHA:91491Congenital ectropion uveae
- ORPHA:566Congenital microcoria
- ORPHA:488197Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome
- ORPHA:250923Isolated aniridia
- ORPHA:519392Isolated iridoschisis
- ORPHA:708Peters anomaly
- ORPHA:91483Rieger anomaly
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98634
- This record as JSON: /data/d/98634.json