| manager |
|
| language |
- |
| license |
- |
| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
|
MONDO_bioport_pref_name
|
183,974 entries
|
There is 0 pattern entry.
|
intellectual disability, autosomal dominant type 39
|
14678 |
|
|
mental retardation, autosomal dominant type 39
|
14678 |
|
|
spastic paraplegia-50, autosomal recessive
|
C567858 |
|
|
craniosynostosis radial aplasia syndrome
|
C536788 |
|
|
recurrent pneumonia, bronchiectasis, and yellowed nails lymphedema of the lower extremities
|
C538678 |
|
|
XP, group c
|
C567886 |
|
|
complementation group c xeroderma pigmentosum
|
C567886 |
|
|
infections, gram-negative bacterial
|
21678 |
|
|
gram negative bacterial infections
|
21678 |
|
|
myopathy, myofibrillar, bag3-related
|
C567843 |
|
|
infiltrating transitional cell carcinoma of the urinary tract
|
40678 |
|
|
vitamin K deficiency bleeding in newborn
|
6784 |
|
|
Helicobacter pylori caused disease or disorder
|
6781 |
|
|
developmental delay, coarse facies, and early death growth retardation
|
C567856 |
|
|
infiltrating urothelial carcinoma
|
40678 |
|
