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loading...| Preferred Name |
Autosomal dominant keratitis |
|
| Synonyms |
Hereditary keratitis |
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| Definitions |
Hereditary keratitis is characterised by opacification and vascularisation of the cornea, often associated with macula hypoplasia. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_2334 |
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| alternative_term |
Hereditary keratitis |
|
| definition |
Hereditary keratitis is characterised by opacification and vascularisation of the cornea, often associated with macula hypoplasia. |
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| definition_citation |
Orphanet |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2334 |
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| has_age_of_onset |
Childhood |
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| has_inheritance |
Autosomal dominant |
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| hasDbXref |
OMIM:148190 UMLS:C1835698 ICD-11:9A7Y MeSH:C537022 ICD-10:H16.8 |
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| label |
Autosomal dominant keratitis |
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| notation |
ORPHA:2334 |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_2334 |
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| prefLabel |
Autosomal dominant keratitis |
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| present_in |
Worldwide AND has_point_prevalence_range : Unknown |
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| treeView | ||
| subClassOf |
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