Current Data About
Troyer syndrome
| (P31) |
(Q929833)
(Q112193867) |
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| (P279) |
(Q657516)
(Q55345926)
(Q200779)
(Q10267817)
|
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| (P1692) |
335.29
|
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| (P1995) |
(Q83042)
|
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| (P2293) |
(Q18036731)
|
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0050886
http://identifiers.org/doid/DOID:0050886
http://www.orpha.net/ORDO/Orphanet_101000 |
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| (P5008) |
(Q4099686)
|
other details
| aliases |
spastic paraplegia 20 (Troyer syndrome) spastic paraplegia type 20 autosomal recessive spastic paraplegia Troyer type autosomal recessive spastic paraplegia 20 autosomal recessive spastic paraplegia type 20 childhood-onset spastic paraparesis with distal muscle wasting SPG20 hereditary spastic paraplegia 20 spastic paraplegia 20 Spastic Paraplegia, Autosomal Recessive, Troyer Type SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20 Spastic paraplegia 20, autosomal recessive Troyer Syndrome Childhood-onset spastic paraparesis-distal muscle wasting syndrome Spastic Paraparesis, Childhood-Onset, With Distal Muscle Wasting Cross-McKusick syndrome |
| description | gene (13q13.1), which encodes the protein spartin. |
External Links
| (P486) |
C536858
|
| (P492) |
275900
|
| (P699) |
DOID:0050886
|
| (P1550) |
101000
|
| (P2892) |
C0393559
|
| (P4229) |
G11.4
|
| (P4317) |
5372
|
| (P5270) |
MONDO_0010156
|
| (P7464) |
troyer-syndrome
|
| (P11430) |
DI-01047
|