|
polyneuropathy organomegalies
|
D016878 |
|
|
partial deletion of chromosome 16
|
16878 |
|
|
polyneuropathy, organomegaly, endocrinopathy, m protein, and skin changes syndrome
|
D016878 |
|
|
partial deletion of chromosome type 16
|
16878 |
|
|
Moraxellaceae infectious disease
|
6878 |
|
|
neonatal severe, due to mecp2 mutations encephalopathy
|
C566878 |
|
|
organomegaly, endocrinopathy, m protein, and skin changes syndrome polyneuropathy
|
D016878 |
|
|
mecp2-related severe neonatal encephalopathy
|
C566878 |
|
|
Moraxellaceae caused disease or disorder
|
6878 |
|
|
partial monosomy of chromosome 16
|
16878 |
|
|
encephalopathy, neonatal severe, due to mecp2 mutations
|
C566878 |
|
