| 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.
|
Pigmented hairy epidermal nevus
|
Orphanet_64755 |
|
|
CANT1-related multiple epiphyseal dysplasia
|
Orphanet_647676 |
|
|
Charcot-Marie-Tooth disease-pyramidal features syndrome
|
Orphanet_64751 |
|
|
Keratitis fugax hereditaria
|
Orphanet_647815 |
|
|
Keratoendotheliitis fugax hereditaria
|
Orphanet_647815 |
|
|
Pregnancy and lactation-associated osteoporosis
|
Orphanet_647823 |
|
|
Idiopathic granulomatous mastitis
|
Orphanet_64722 |
|
|
X-linked hereditary motor and sensory neuropathy
|
Orphanet_64747 |
|
|
Polymorphic eruption of pregnancy
|
Orphanet_64745 |
|
|
Idiopathic pregnancy-associated osteoporosis
|
Orphanet_647823 |
|
|
Pregnancy induced osteoporosis
|
Orphanet_647823 |
|
|
Idiopathic premenopausal osteoporosis associated with pregnancy
|
Orphanet_647823 |
|
|
Pruritic urticarial papules and plaques of pregnancy
|
Orphanet_64745 |
|
|
Isolated primary pigmented nodular adrenocortical disease
|
Orphanet_647772 |
|
|
Osteoporosis of pregnancy
|
Orphanet_647823 |
|
