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Ontology Browser
Term:
Spastic Paraplegia 91, Autosomal Dominant, with or without Cerebellar Ataxia (DOID:9008626)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1) Naked Mole-rat: (1) Green Monkey: (1)
Parent Terms Term With Siblings Child Terms
3-methylglutaconic aciduria type 3  
Amyotrophic Dystonic Paraplegia 
Arena Syndrome 
Bahemuka Brown Syndrome 
Distal Transverse Limb Defects with Mental Retardation and Spasticity 
early-onset dystonia and/or spastic paraplegia  
Fitzsimmons Walson Mellor Syndrome 
Fitzsimmons-Guilbert Syndrome 
Fitzsimmons-McLachlan-Gilbert syndrome 
Hereditary Spastic Paralysis, Infantile Onset Ascending  
hereditary spastic paraplegia 10  
hereditary spastic paraplegia 11  
hereditary spastic paraplegia 12  
hereditary spastic paraplegia 13  
hereditary spastic paraplegia 14 
hereditary spastic paraplegia 15  
hereditary spastic paraplegia 16 
hereditary spastic paraplegia 17  
hereditary spastic paraplegia 18  
hereditary spastic paraplegia 19 
hereditary spastic paraplegia 2  
hereditary spastic paraplegia 23  
hereditary spastic paraplegia 24 
hereditary spastic paraplegia 25 
hereditary spastic paraplegia 26  
hereditary spastic paraplegia 27 
hereditary spastic paraplegia 28  
hereditary spastic paraplegia 29 
hereditary spastic paraplegia 30 +   
hereditary spastic paraplegia 31  
hereditary spastic paraplegia 32 
hereditary spastic paraplegia 33  
hereditary spastic paraplegia 34 
hereditary spastic paraplegia 35  
hereditary spastic paraplegia 36 
hereditary spastic paraplegia 37 
hereditary spastic paraplegia 38 
hereditary spastic paraplegia 39  
hereditary spastic paraplegia 3A  
hereditary spastic paraplegia 4  
hereditary spastic paraplegia 41 
hereditary spastic paraplegia 42  
hereditary spastic paraplegia 43  
hereditary spastic paraplegia 44  
hereditary spastic paraplegia 45  
hereditary spastic paraplegia 46  
hereditary spastic paraplegia 47  
hereditary spastic paraplegia 48  
hereditary spastic paraplegia 49  
hereditary spastic paraplegia 50  
hereditary spastic paraplegia 51  
hereditary spastic paraplegia 52  
hereditary spastic paraplegia 53  
hereditary spastic paraplegia 54  
hereditary spastic paraplegia 55  
hereditary spastic paraplegia 56  
hereditary spastic paraplegia 57  
hereditary spastic paraplegia 5A  
hereditary spastic paraplegia 6  
hereditary spastic paraplegia 61  
hereditary spastic paraplegia 62  
hereditary spastic paraplegia 63  
hereditary spastic paraplegia 64  
hereditary spastic paraplegia 7  
hereditary spastic paraplegia 70  
hereditary spastic paraplegia 72A  
hereditary spastic paraplegia 73  
hereditary spastic paraplegia 74  
hereditary spastic paraplegia 75  
hereditary spastic paraplegia 76  
hereditary spastic paraplegia 77  
hereditary spastic paraplegia 78  
hereditary spastic paraplegia 79A  
hereditary spastic paraplegia 79B  
hereditary spastic paraplegia 8  
hereditary spastic paraplegia 80  
hereditary spastic paraplegia 81  
hereditary spastic paraplegia 82  
hereditary spastic paraplegia 83  
hereditary spastic paraplegia 84  
hereditary spastic paraplegia 85  
hereditary spastic paraplegia 86  
hereditary spastic paraplegia 87  
hereditary spastic paraplegia 88  
hereditary spastic paraplegia 89  
hereditary spastic paraplegia 90A  
hereditary spastic paraplegia 90B  
hereditary spastic paraplegia 9A  
hereditary spastic paraplegia 9B  
MASA syndrome  
MAST syndrome  
Mental Retardation Spasticity Ectrodactyly 
NEURODEVELOPMENTAL DISORDER WITH MOTOR REGRESSION, PROGRESSIVE SPASTIC PARAPLEGIA, AND OROMOTOR DYSFUNCTION  
Roy Maroteaux Kremp Syndrome 
spastic ataxia 1  
spastic ataxia 2  
spastic ataxia 3  
Spastic Diplegia Infantile Type 
Spastic Paraplegia 91, Autosomal Dominant, with or without Cerebellar Ataxia  
A highly variable neurologic disorder characterized by early-onset gait abnormalities due to spastic paraplegia of the lower limbs, sometimes with cerebellar ataxia. Caused by heterozygous mutation in the SPTAN1 gene on chromosome 9q34.
Spastic Paraplegia 92, Autosomal Recessive  
Spastic Paraplegia and Evans Syndrome 
Spastic Paraplegia Type 5B, Recessive 
Spastic Paraplegia with Associated Extrapyramidal Signs 
spastic paraplegia with deafness 
Spastic Paraplegia with Kallmann Syndrome 
Spastic Paraplegia with Myoclonic Epilepsy 
Spastic Paraplegia with Neuropathy and Poikiloderma 
Spastic Paraplegia with Precocious Puberty 
Spastic Paraplegia, Epilepsy, Mental Retardation 
SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY  
Spastic Paraplegia, Optic Atrophy, and Dementia 
Spastic Paraplegia, Optic Atrophy, Microcephaly, and XY Sex Reversal 
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 
SPASTIC TETRAPLEGIA AND AXIAL HYPOTONIA, PROGRESSIVE  
spastic tetraplegia, thin corpus callosum, and progressive microcephaly  
Troyer syndrome  
Volcke Soekarman Syndrome 

Synonyms
Exact Synonyms: SPG91
Primary IDs: MIM:620538
Definition Sources: MIM:620538

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