Disease Browser
Parent Node: Paraplegia (D010264) Parent Node: Spastic Paraplegia, Hereditary (D015419) ..Starting node .. Spastic Paraplegia Type 11 (C580453) Child Nodes:
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) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 10411
Name: Spastic Paraplegia Type 11
Definition:
Alternative IDs:
ParentIDs: MESH:D010264|MESH:D015419
TreeNumbers: C10.500.300.820/C580453 |C10.574.500.495.820/C580453 |C10.597.622.669/C580453 |C10.668.829.800.300.820/C580453 |C16.131.666.300.820/C580453 |C16.320.400.375.820/C580453 |C23.888.592.636.637/C580453
Synonyms: Autosomal Recessive Spastic Paraplegia Complicated with Thin Corpus Callosum |Autosomal Recessive Spastic Paraplegia with Mental Impairment and Thin Corpus Callosum |Hsp-Tcc |Spg11-Related Hereditary Spastic Paraplegia with Thin Corpus Callosum
Slim Mappings: Congenital abnormality|Genetic disease (inborn)|Nervous system disease|Signs and symptoms
Reference:
MedGen: C580453
MeSH: C580453
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants