|
intellectual disability, X-linked, syndromic, Houge type
|
30909 |
|
|
mental retardation, X-linked, syndromic, Houge type
|
30909 |
|
|
infection by Yersinia pestis
|
19095 |
|
|
postaxial, type a4 polydactyly
|
C563909 |
|
|
Bartholin gland adenomyoma
|
3909 |
|
|
retinal nonattachment and falciform detachment
|
9097 |
|
|
obsolete meconium aspiration syndrome
|
19090.0 |
|
|
deafness, sensorineural, autosomal-mitochondrial type
|
9090 |
|
|
UV-sensitive syndrome caused by mutation in ERCC6
|
10909 |
|
|
Charcot-Marie-Tooth disease caused by mutation in MPZ
|
11909 |
|
|
glioblastomas, giant cell
|
D005909 |
|
