| 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.
|
hidrotic, autosomal recessive ectodermal dysplasia
|
C566553 |
|
|
type a2 postaxial polydactyly
|
C566585 |
|
|
generalized lichenoid papular eruption
|
15665 |
|
|
facial nerve paralysis
|
5665 |
|
|
autosomal dominant parkinson disease 3
|
C566552 |
|
|
idiopathic intestinal pseudoobstruction
|
C566502 |
|
|
hypospadias, and penoscrotal inversion anal atresia
|
C566526 |
|
|
congenital, autosomal recessive fibrosis of extraocular muscles
|
C566587 |
|
|
selective, 2 tooth agenesis
|
C566513 |
|
|
shohat type spondyloepimetaphyseal dysplasia
|
C566523 |
|
|
missouri type spondyloepimetaphyseal dysplasia
|
C566574 |
|
|
intestinal, with secondary hypocalcemia hypomagnesemia
|
C566593 |
|
|
congenital, with synergistic divergence fibrosis of extraocular muscles
|
C566508 |
|
|
ectodermal dysplasia, pure hair-nail type
|
C566592 |
|
|
spondyloepimetaphyseal dysplasia, shohat type
|
C566523 |
|
