Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandDeafness (D003638)
Parent Node:
expandSpastic Paraplegia, Hereditary (D015419)
..Starting node
..expandSpastic paraplegia 24 (C536860)

       Child Nodes:



 Sister Nodes: 
..expandAmyotrophic Dystonic Paraplegia (C566292)
..expandArena syndrome (C537428)
..expandAtaxia, Spastic, 1, Autosomal Dominant (C566993)
..expandAtaxia, Spastic, 2, Autosomal Recessive (C566969)
..expandAtaxia, Spastic, 3, Autosomal Recessive (C566956)
..expandBahemuka Brown syndrome (C537797)
..expandCosteff optic atrophy syndrome (C535311)
..expandFitzsimmons Walson Mellor syndrome (C537937)
..expandFitzsimmons-Guilbert syndrome (C537938)
..expandFitzsimmons-McLachlan-Gilbert syndrome (C537058)
..expandHereditary spastic paralysis, infantile onset ascending (C537217)
..expandLeukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia (C567311)
..expandLimb Defects, Distal Transverse, with Mental Retardation and Spasticity (C565438)
..expandMASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome (C536029)
..expandMAST Syndrome (C565409)
..expandMental retardation spasticity ectrodactyly (C537446)
..expandNakamura Osame syndrome (C538335)
..expandRoy Maroteaux Kremp syndrome (C535875)
..expandSpastic diplegia infantile type (C537481)
..expandSpastic paraplegia 10, autosomal dominant (C537482)
..expandSpastic paraplegia 11, autosomal recessive (C537483)
..expandSpastic paraplegia 12, autosomal dominant (C537484)
..expandSpastic paraplegia 13, autosomal dominant (C537485)
..expandSpastic paraplegia 14, autosomal recessive (C537486)
..expandSpastic paraplegia 15, autosomal recessive (C536642)
..expandSpastic paraplegia 16, X-linked (C536643)
..expandSpastic paraplegia 17 (C536644)
..expandSpastic Paraplegia 18, Autosomal Recessive (C567628)
..expandSpastic paraplegia 19, autosomal dominant (C536856)
..expandSpastic paraplegia 2, X-linked (C536857)
..expandSpastic paraplegia 20, autosomal recessive (C536858)
..expandSpastic paraplegia 23 (C536859)
..expandSpastic paraplegia 24 (C536860)
..expandSpastic paraplegia 25, autosomal recessive (C536861)
..expandSpastic paraplegia 26, autosomal recessive (C536862)
..expandSpastic Paraplegia 27, Autosomal Recessive (C563807)
..expandSpastic paraplegia 29, autosomal dominant (C536863)
..expandSpastic paraplegia 3, autosomal dominant (C536864)
..expandSpastic Paraplegia 31, Autosomal Dominant (C565210)
..expandSpastic Paraplegia 32, Autosomal Recessive (C566983)
..expandSpastic Paraplegia 33, Autosomal Dominant (C565214)
..expandSpastic Paraplegia 34, X-Linked (C567465)
..expandSPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE (OMIM:612319)
..expandSpastic Paraplegia 36, Autosomal Dominant (C567930)
..expandSpastic Paraplegia 37, Autosomal Dominant (C567931)
..expandSpastic Paraplegia 38, Autosomal Dominant (C567349)
..expandSpastic Paraplegia 39, Autosomal Recessive (C567433)
..expandSpastic paraplegia 4, autosomal dominant (C536865)
..expandSPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT (OMIM:613364)
..expandSpastic Paraplegia 42, Autosomal Dominant (C567262)
..expandSpastic Paraplegia 44, Autosomal Recessive (C567707)
..expandSPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE (OMIM:613162)
..expandSPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE (OMIM:613647)
..expandSPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE (OMIM:615031)
..expandSpastic Paraplegia 5a, Autosomal Recessive (C564811)
..expandSpastic paraplegia 6, autosomal dominant (C536866)
..expandSpastic Paraplegia 7, Autosomal Recessive (C564599)
..expandSpastic paraplegia 8, autosomal dominant (C536867)
..expandSpastic paraplegia 9, autosomal dominant (C536868)
..expandSpastic Paraplegia And Evans Syndrome (C566652)
..expandSpastic paraplegia epilepsy mental retardation (C536869)
..expandSpastic paraplegia neuropathy poikiloderma (C536870)
..expandSpastic Paraplegia Type 11 (C580453)
..expandSpastic Paraplegia Type 3a (C580455)
..expandSpastic Paraplegia Type 4 (C580456)
..expandSpastic paraplegia type 5A, recessive (C536871)
..expandSpastic paraplegia type 5B, recessive (C536872)
..expandSpastic Paraplegia Type 7 (C580457)
..expandSpastic Paraplegia Type 8 (C580458)
..expandSpastic Paraplegia With Associated Extrapyramidal Signs (C566681)
..expandSpastic paraplegia with Kallmann syndrome (C536873)
..expandSpastic Paraplegia With Myoclonic Epilepsy (C564810)
..expandSpastic paraplegia with precocious puberty (C536874)
..expandSpastic Paraplegia, Optic Atrophy, And Dementia (C566679)
..expandSpastic Paraplegia, Optic Atrophy, Microcephaly, And Xy Sex Reversal (C566409)
..expandSpastic Paraplegia, Sensorineural Deafness, Mental Retardation, And Progressive Nephropathy (C566682)
..expandSpastic Paraplegia-50, Autosomal Recessive (C567858)
..expandVolcke Soekarman syndrome (C537718)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:10370
Name:Spastic paraplegia 24
Definition:
Alternative IDs:OMIM:607584
ParentIDs:MESH:D003638|MESH:D015419
TreeNumbers:C09.218.458.341.186/C536860 |C10.500.300.820/C536860 |C10.574.500.495.820/C536860 |C10.597.751.418.341.186/C536860 |C10.668.829.800.300.820/C536860 |C16.131.666.300.820/C536860 |C16.320.400.375.820/C536860 |C23.888.592.763.393.341.186/C536860
Synonyms:SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE |SPG24
Slim Mappings:Congenital abnormality|Ear-nose-throat disease|Genetic disease (inborn)|Nervous system disease|Signs and symptoms
Reference: MedGen: C536860
MeSH: C536860
OMIM: 607584;

Genes: SPG24;
Phenotypes
1 HP:0000007Autosomal recessive inheritance
2 HP:0003593Infantile onset
3 HP:0002169Clonus
4 HP:0003698Difficulty standing
5 HP:0001258Spastic paraplegia
6 HP:0001257Spasticity
7 HP:0030051Tip-toe gait
Disease Causing ClinVar Variants