manager |
|
language |
- |
license |
- |
created at |
2017-12-21 11:07:44 UTC |
updated at |
2017-12-22 12:31:05 UTC |
|
2 layers
|
520,470 entries
|
There is 0 pattern entry.
Osteogenesis Imperfecta, Type IIB
|
DISO:MSH |
|
Osteoglophonic dwarfism
|
DISO:MSH |
|
Osteoglophonic dysplasia
|
DISO:MSH |
|
Fairbank-Keats syndrome
|
DISO:MSH |
|
Winchester-Grossman syndrome
|
DISO:MSH |
|
Winchester syndrome
|
DISO:MSH |
|
Winchester-Grossman disease
|
DISO:MSH |
|
Winchester disease
|
DISO:MSH |
|
McCabe disease
|
DISO:MSH |
|
Expansile osteolysis, familial
|
DISO:MSH |
|
Familial expansile osteolysis
|
DISO:MSH |
|
Osteolysis, familial expansile
|
DISO:MSH |
|
Polyostotic osteolytic dysplasia, hereditary expansile
|
DISO:MSH |
|
Lamellar ichthyosis, autosomal dominant form
|
DISO:MSH |
|
Ichthyosiform erythroderma, nonbullous, dominant form
|
DISO:MSH |
|