| manager |
|
| language |
- |
| license |
- |
| created at |
2019-07-11 18:15:35 UTC |
| updated at |
2025-12-23 18:38:35 UTC |
|
Diseases and disorders as defined in the MONDO ontology, the version 2025-01-07.
Only the terms under the node "disease" (MONDO_0000001) are included.
All identifiers use the CURIE format with the MONDO: prefix (e.g., MONDO:12345),
which corresponds to the full IRI namespace http://purl.obolibrary.org/obo/MONDO_.
|
112,359 entries
|
There is 0 pattern entry.
|
familial TTP
|
MONDO:0010122 |
|
|
Upshaw Factor, deficiency of
|
MONDO:0010122 |
|
|
congenital thrombotic thrombocytopenic purpura
|
MONDO:0010122 |
|
|
thrombotic microangiopathy, familial
|
MONDO:0010122 |
|
|
thrombotic thrombocytopenic purpura, congenital
|
MONDO:0010122 |
|
|
TTP, congenital
|
MONDO:0010122 |
|
|
thrombotic thrombocytopenic purpura, familial
|
MONDO:0010122 |
|
|
Microangiopathic hemolytic Anemia, congenital
|
MONDO:0010122 |
|
|
Microangiopathic hemolytic Anemia
|
MONDO:0010122 |
|
|
Microangiopathic hemolytic Anaemia
|
MONDO:0010122 |
|
|
Schulman-Upshaw syndrome
|
MONDO:0010122 |
|
|
hereditary thrombotic thrombocytopenic purpura
|
MONDO:0010122 |
|
|
congenital TTP
|
MONDO:0010122 |
|
|
Upshaw-Schulman syndrome
|
MONDO:0010122 |
|
|
congenital ADAMTS-13 deficiency
|
MONDO:0010122 |
|
