Disease Browser
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Parent Node: Spastic Paraplegia, Hereditary (D015419) | ..Starting node ..Spastic paraplegia 8, autosomal dominant (C536867)
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Sister Nodes: | ..Amyotrophic Dystonic Paraplegia (C566292)
| ..Arena syndrome (C537428)
| ..Ataxia, Spastic, 1, Autosomal Dominant (C566993)
| ..Ataxia, Spastic, 2, Autosomal Recessive (C566969)
| ..Ataxia, Spastic, 3, Autosomal Recessive (C566956)
| ..Bahemuka Brown syndrome (C537797)
| ..Costeff optic atrophy syndrome (C535311)
| ..Fitzsimmons Walson Mellor syndrome (C537937)
| ..Fitzsimmons-Guilbert syndrome (C537938)
| ..Fitzsimmons-McLachlan-Gilbert syndrome (C537058)
| ..Hereditary spastic paralysis, infantile onset ascending (C537217)
| ..Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia (C567311)
| ..Limb Defects, Distal Transverse, with Mental Retardation and Spasticity (C565438)
| ..MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome (C536029)
| ..MAST Syndrome (C565409)
| ..Mental retardation spasticity ectrodactyly (C537446)
| ..Nakamura Osame syndrome (C538335)
| ..Roy Maroteaux Kremp syndrome (C535875)
| ..Spastic diplegia infantile type (C537481)
| ..Spastic paraplegia 10, autosomal dominant (C537482)
| ..Spastic paraplegia 11, autosomal recessive (C537483)
| ..Spastic paraplegia 12, autosomal dominant (C537484)
| ..Spastic paraplegia 13, autosomal dominant (C537485)
| ..Spastic paraplegia 14, autosomal recessive (C537486)
| ..Spastic paraplegia 15, autosomal recessive (C536642)
| ..Spastic paraplegia 16, X-linked (C536643)
| ..Spastic paraplegia 17 (C536644)
| ..Spastic Paraplegia 18, Autosomal Recessive (C567628)
| ..Spastic paraplegia 19, autosomal dominant (C536856)
| ..Spastic paraplegia 2, X-linked (C536857)
| ..Spastic paraplegia 20, autosomal recessive (C536858)
| ..Spastic paraplegia 23 (C536859)
| ..Spastic paraplegia 24 (C536860)
| ..Spastic paraplegia 25, autosomal recessive (C536861)
| ..Spastic paraplegia 26, autosomal recessive (C536862)
| ..Spastic Paraplegia 27, Autosomal Recessive (C563807)
| ..Spastic paraplegia 29, autosomal dominant (C536863)
| ..Spastic paraplegia 3, autosomal dominant (C536864)
| ..Spastic Paraplegia 31, Autosomal Dominant (C565210)
| ..Spastic Paraplegia 32, Autosomal Recessive (C566983)
| ..Spastic Paraplegia 33, Autosomal Dominant (C565214)
| ..Spastic Paraplegia 34, X-Linked (C567465)
| ..SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE (OMIM:612319)
| ..Spastic Paraplegia 36, Autosomal Dominant (C567930)
| ..Spastic Paraplegia 37, Autosomal Dominant (C567931)
| ..Spastic Paraplegia 38, Autosomal Dominant (C567349)
| ..Spastic Paraplegia 39, Autosomal Recessive (C567433)
| ..Spastic paraplegia 4, autosomal dominant (C536865)
| ..SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT (OMIM:613364)
| ..Spastic Paraplegia 42, Autosomal Dominant (C567262)
| ..Spastic Paraplegia 44, Autosomal Recessive (C567707)
| ..SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE (OMIM:613162)
| ..SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE (OMIM:613647)
| ..SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE (OMIM:615031)
| ..Spastic Paraplegia 5a, Autosomal Recessive (C564811)
| ..Spastic paraplegia 6, autosomal dominant (C536866)
| ..Spastic Paraplegia 7, Autosomal Recessive (C564599)
| ..Spastic paraplegia 8, autosomal dominant (C536867)
| ..Spastic paraplegia 9, autosomal dominant (C536868)
| ..Spastic Paraplegia And Evans Syndrome (C566652)
| ..Spastic paraplegia epilepsy mental retardation (C536869)
| ..Spastic paraplegia neuropathy poikiloderma (C536870)
| ..Spastic Paraplegia Type 11 (C580453)
| ..Spastic Paraplegia Type 3a (C580455)
| ..Spastic Paraplegia Type 4 (C580456)
| ..Spastic paraplegia type 5A, recessive (C536871)
| ..Spastic paraplegia type 5B, recessive (C536872)
| ..Spastic Paraplegia Type 7 (C580457)
| ..Spastic Paraplegia Type 8 (C580458)
| ..Spastic Paraplegia With Associated Extrapyramidal Signs (C566681)
| ..Spastic paraplegia with Kallmann syndrome (C536873)
| ..Spastic Paraplegia With Myoclonic Epilepsy (C564810)
| ..Spastic paraplegia with precocious puberty (C536874)
| ..Spastic Paraplegia, Optic Atrophy, And Dementia (C566679)
| ..Spastic Paraplegia, Optic Atrophy, Microcephaly, And Xy Sex Reversal (C566409)
| ..Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, And Progressive Nephropathy (C566682)
| ..Spastic Paraplegia-50, Autosomal Recessive (C567858)
| ..Volcke Soekarman syndrome (C537718)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 10400 |
Name: | Spastic paraplegia 8, autosomal dominant |
Definition: | |
Alternative IDs: | OMIM:603563 |
ParentIDs: | MESH:D015419 |
TreeNumbers: | C10.500.300.820/C536867 |C10.574.500.495.820/C536867 |C10.668.829.800.300.820/C536867 |C16.131.666.300.820/C536867 |C16.320.400.375.820/C536867 |
Synonyms: | SPG8 |
Slim Mappings: | Congenital abnormality|Genetic disease (inborn)|Nervous system disease |
Reference: |
MedGen: C536867
MeSH: C536867
OMIM: 603563;
Genes: KIAA0196; | Phenotypes | | Disease Causing ClinVar Variants | Variation_Name | GeneID | GeneSymbol | ClinicalSignificance | dbSNP | RCVaccession | TestedInGTR | PhenotypeIDs | Chromosome | Start | Stop | HGVS_c | HGVS_p | HGVS_g | OtherIDs | Disease_ClinVar | Disease_hgmd | NM_014846.3(KIAA0196):c.2087G>C (p.Gly696Ala) | 9897 | KIAA0196 | Pathogenic | 397515564 | RCV000055943; | N | MedGen:C1863704,OMIM:603563,ORPHA:100989 | 8 | 126067843 | 126067843 | NM_014846.3:c.2087G>C | NP_055661.3:p.Gly696Ala | NC_000008.10:g.126067843C>G | OMIM Allelic Variant:610657.0005 | C1863704 603563 Spastic paraplegia 8 | | | NM_014846.3(KIAA0196):c.1876G>T (p.Val626Phe) | 9897 | KIAA0196 | Pathogenic | 80338867 | RCV000001220; | N | MedGen:C1863704,OMIM:603563,ORPHA:100989 | 8 | 126069059 | 126069059 | NM_014846.3:c.1876G>T | NP_055661.3:p.Val626Phe | NC_000008.10:g.126069059C>A | OMIM Allelic Variant:610657.0001 | C1863704 603563 Spastic paraplegia 8 | | | NM_014846.3(KIAA0196):c.1857G>C (p.Leu619Phe) | 9897 | KIAA0196 | Pathogenic | 80338866 | RCV000001221; | N | MedGen:C1863704,OMIM:603563,ORPHA:100989 | 8 | 126069816 | 126069816 | NM_014846.3:c.1857G>C | NP_055661.3:p.Leu619Phe | NC_000008.10:g.126069816C>A,NC_000008.10:g.126069816C>G | OMIM Allelic Variant:610657.0002 | C1863704 603563 Spastic paraplegia 8 | | | NM_014846.3(KIAA0196):c.1857G>T (p.Leu619Phe) | 9897 | KIAA0196 | Pathogenic | 80338866 | RCV000032101; | N | MedGen:C1863704,OMIM:603563,ORPHA:100989 | 8 | 126069816 | 126069816 | NM_014846.3:c.1857G>T | NP_055661.3:p.Leu619Phe | NC_000008.10:g.126069816C>A,NC_000008.10:g.126069816C>G | - | C1863704 603563 Spastic paraplegia 8 | | | NM_014846.3(KIAA0196):c.1411A>G (p.Asn471Asp) | 9897 | KIAA0196 | Pathogenic | 80338865 | RCV000001222; | N | MedGen:C1863704,OMIM:603563,ORPHA:100989 | 8 | 126073434 | 126073434 | NM_014846.3:c.1411A>G | NP_055661.3:p.Asn471Asp | NC_000008.10:g.126073434T>C | OMIM Allelic Variant:610657.0003 | C1863704 603563 Spastic paraplegia 8 | | |
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