Troyer syndrome
gene (13q13.1), which encodes the protein spartin.
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Troyer syndrome
Summary
Troyer syndrome is a rare disease[1]. It is known by 19 alternative names across languages and contexts.[2]
Key Facts
- Troyer syndrome's instance of is recorded as rare disease[3].
- Troyer syndrome's instance of is recorded as class of disease[4].
- Troyer syndrome is a type of hereditary spastic paraplegia[5].
- Troyer syndrome is a type of autosomal recessive complex spastic paraplegia[6].
- Troyer syndrome is a type of genetic disease[7].
- Troyer syndrome is a type of autosomal recessive disease[8].
- Troyer syndrome's ICD-9-CM is recorded as 335.29[9].
- Troyer syndrome's health specialty is recorded as neurology[10].
- Troyer syndrome's genetic association is recorded as SPART[11].
- Troyer syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050886[12].
- Troyer syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050886[13].
- Troyer syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101000[14].
- Troyer syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
Troyer syndrome is known by 19 alternative names across languages and contexts.[2]