Current Data About
Werdnig–Hoffmann disease
| (P31) |
(Q929833)
(Q2246789) (Q112193867) |
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| (P138) |
(Q87534)
(Q91264) |
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| (P279) |
(Q50357578)
|
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| (P1692) |
335.0
|
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| (P1748) |
C98670
|
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| (P1995) |
(Q83042)
|
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| (P2293) |
(Q18031604)
|
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_13137
http://identifiers.org/doid/DOID:13137
|
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| (P5008) |
(Q4099686)
|
other details
| aliases |
Werdnig–Hoffmann syndrome Werdnig-Hoffmann disease infantile muscular atrophy progressive muscular atrophy of infancy Werdnig-Hoffman disease spinal muscular atrophy type 1 HMN (Hereditary motor Neuropathy) Proximal type I hereditary motor neuropathy proximal type I Spinal muscular atrophy 1 SMA1 |
| description | Human disease |
External Links
| (P268) |
13514535n
|
| (P492) |
253300
|
| (P508) |
55551
|
| (P699) |
DOID:13137
|
| (P2892) |
C0043116
|
| (P4229) |
G12.0
|
| (P4233) |
spinal-muscular-atrophy-type-1
|
| (P4317) |
7883
|
| (P5270) |
MONDO_0009669
|
| (P11430) |
DI-01055
|