|
intracranial primitive neuroectodermal neoplasm
|
3142 |
|
|
hereditary sensory and autonomic neuropathy type 2 caused by mutation in RETREG1
|
13142 |
|
|
hereditary sensory and autonomic neuropathy type 2B
|
13142 |
|
|
hereditary sensory and autonomic neuropathy type IIB
|
13142 |
|
|
fetal brain disruption sequence
|
23142 |
|
|
x-linked 20 mental retardation
|
C563142 |
|
|
brain primitive neuroectodermal tumor
|
3142 |
|
|
intracranial primitive neuroectodermal tumor
|
3142 |
|
|
primitive neuroectodermal tumor of brain
|
3142 |
|
|
RETREG1 hereditary sensory and autonomic neuropathy type 2
|
13142 |
|
|
neuropathy, hereditary sensory and autonomic, type 2B
|
13142 |
|
|
neuropathy, hereditary sensory and autonomic, type IIB
|
13142 |
|
|
neuropathy, hereditary sensory and autonomic, type IIB; HSAN2B
|
http://purl.obolibrary.org/obo/MONDO_0013142 |
|
