loading...| Preferred Name |
Nanophthalmos |
| ID |
http://www.orpha.net/ORDO/Orphanet_35612 |
| alternative_term |
Nanophthalmia |
| definition |
A rare ophthalmic disease and a severe form of microphthalmia (small eye phenotype) characterized by a small eye with a short axial length, severe hyperopia, an elevated lens/eye ratio, and a high incidence of angle-closure glaucoma. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=35612 |
| has_age_of_onset |
Neonatal Infancy |
| has_inheritance |
Autosomal recessive Not applicable Autosomal dominant |
| hasDbXref |
OMIM:600165 OMIM:615972 ICD-10:Q11.2 ICD-11:LA10.0 OMIM:611897 OMIM:613517 OMIM:609549 |
| label |
Nanophthalmos |
| notation |
ORPHA:35612 |
| part_of |
http://www.orpha.net/ORDO/Orphanet_98683 http://www.orpha.net/ORDO/Orphanet_522520 http://www.orpha.net/ORDO/Orphanet_98631 |
| prefixIRI |
ORDO:Orphanet_35612 |
| prefLabel |
Nanophthalmos |
| present_in |
Worldwide AND has_point_prevalence_range : Unknown |
| treeView |
http://www.orpha.net/ORDO/Orphanet_98683 http://www.orpha.net/ORDO/Orphanet_522520 http://www.orpha.net/ORDO/Orphanet_98631 |
| subClassOf |