manager |
|
language |
- |
license |
- |
created at |
2024-09-23 16:23:50 UTC |
updated at |
2024-09-23 18:22:39 UTC |
|
Terms for rare diseases as defined in ORDO.
The entries were initially sourced from the ORDO version 2024-07-03 as stored in BioPortal.
Namespace: http://www.orpha.net/ORDO/
|
20,514 entries
|
There is 0 pattern entry.
Complete atrioventricular septal defect-tetralogy of Fallot
|
Orphanet_99068 |
|
Aorto-right ventricular tunnel
|
Orphanet_99070 |
|
Aorto-left ventricular tunnel
|
Orphanet_99071 |
|
Cor triatriatum sinistrum
|
Orphanet_99099 |
|
DORV, Fallot type
|
Orphanet_99043 |
|
APV/PDA, non-Fallot type
|
Orphanet_99048 |
|
HMSN, Lom type
|
Orphanet_99950 |
|
Unroofed coronary sinus
|
Orphanet_99104 |
|
ASD, coronary sinus type
|
Orphanet_99104 |
|
Autosomal dominant spinocerebellar ataxia
|
Orphanet_99 |
|
Pena-Shokeir syndrome type 1
|
Orphanet_994 |
|
Pleuropulmonary blastoma type 1
|
Orphanet_99933 |
|
Atypical PSP syndrome
|
Orphanet_99750 |
|
Agnathia-holoprosencephaly-situs inversus syndrome
|
Orphanet_990 |
|
Tarsal kink syndrome
|
Orphanet_99170 |
|