| manager |
|
| language |
- |
| license |
- |
| created at |
2021-12-23 02:14:06 UTC |
| updated at |
2021-12-23 14:43:01 UTC |
|
"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
|
82,725 entries
|
There is 0 pattern entry.
|
neuropathy, hereditary sensory and autonomic, type i
|
D009477 |
|
|
neuropathy, hereditary sensory and autonomic, type v
|
D009477 |
|
|
HSAN (hereditary sensory autonomic neuropathy)
|
D009477 |
|
|
HSANs (hereditary sensory autonomic neuropathy)
|
D009477 |
|
|
neuropathy hereditary sensory radicular, autosomal dominant
|
D009477 |
|
|
neuropathy, hereditary sensory radicular, autosomal dominant
|
D009477 |
|
|
neuropathy, hereditary sensory radicular, autosomal recessive
|
D009477 |
|
|
neuropathy, progressive sensory, of children
|
D009477 |
|
|
neuropathy, hereditary sensory, type i
|
D009477 |
|
|
neuropathy, congenital sensory, with anhidrosis
|
D009477 |
|
|
hereditary sensory radicular neuropathy, recessive form
|
D009477 |
|
|
hereditary sensory radicular, autosomal dominant neuropathy
|
D009477 |
|
|
hereditary sensory radicular, autosomal recessive neuropathy
|
D009477 |
|
|
acroosteolysis, giaccai type
|
D009477 |
|
|
congenital insensitivity to pain with anhidrosis
|
D009477 |
|
