Preferred Name

Friedreich ataxia
Synonyms

hereditary spinal ataxia

Friedreich ataxia with retained reflexes

spinocerebellar ataxia, Friedreich

hereditary spinal sclerosis

FRDA

FA

Friedreich's ataxia

Friedreich ataxia

Friedreich's tabes

Definitions

An inherited condition that affects the nervous system and causes movement problems. People with this condition develop impaired muscle coordination (ataxia) that worsens over time. Other features include the gradual loss of strength and sensation in the arms and legs, muscle stiffness (spasticity), and impaired speech. Many individuals have a form of heart disease called hypertrophic cardiomyopathy. Some develop diabetes, impaired vision, hearing loss, or an abnormal curvature of the spine (scoliosis). Most people with Friedreich ataxia begin to experience the signs and symptoms around puberty.

ID

http://purl.obolibrary.org/obo/MONDO_0100339

altLabel

hereditary spinal ataxia

Friedreich ataxia with retained reflexes

spinocerebellar ataxia, Friedreich

hereditary spinal sclerosis

FRDA

FA

Friedreich's ataxia

Friedreich ataxia

Friedreich's tabes

created_by

https://orcid.org/0000-0001-5208-3432

definition

An inherited condition that affects the nervous system and causes movement problems. People with this condition develop impaired muscle coordination (ataxia) that worsens over time. Other features include the gradual loss of strength and sensation in the arms and legs, muscle stiffness (spasticity), and impaired speech. Many individuals have a form of heart disease called hypertrophic cardiomyopathy. Some develop diabetes, impaired vision, hearing loss, or an abnormal curvature of the spine (scoliosis). Most people with Friedreich ataxia begin to experience the signs and symptoms around puberty.

has_exact_synonym

FRDA

FA

Friedreich's ataxia

Friedreich ataxia

Friedreich's tabes

has_related_synonym

hereditary spinal ataxia

Friedreich ataxia with retained reflexes

spinocerebellar ataxia, Friedreich

hereditary spinal sclerosis

label

Friedreich ataxia

prefixIRI

MONDO:0100339

prefLabel

Friedreich ataxia

seeAlso

https://rarediseases.info.nih.gov/diseases/6468/friedreich-ataxia

textual definition

An inherited condition that affects the nervous system and causes movement problems. People with this condition develop impaired muscle coordination (ataxia) that worsens over time. Other features include the gradual loss of strength and sensation in the arms and legs, muscle stiffness (spasticity), and impaired speech. Many individuals have a form of heart disease called hypertrophic cardiomyopathy. Some develop diabetes, impaired vision, hearing loss, or an abnormal curvature of the spine (scoliosis). Most people with Friedreich ataxia begin to experience the signs and symptoms around puberty.

subClassOf

http://purl.obolibrary.org/obo/MONDO_0024573

http://purl.obolibrary.org/obo/MONDO_0015368

http://purl.obolibrary.org/obo/MONDO_0020046

Delete Subject Author Type Created
No notes to display
Create mapping

Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0100339 CCONT SAME_URI
http://purl.obolibrary.org/obo/MONDO_0100339 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0100339 EFO SAME_URI
urn:agi-folder:friedreich_ataxia BPT LOOM
http://www.orpha.net/ORDO/Orphanet_95 ORDO LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038582 PMAPP-PMO LOOM
http://purl.jp/bio/4/id/200906072968387836 IOBC LOOM
http://purl.bioontology.org/ontology/ICD10CM/G11.11 ICD10CM LOOM
http://purl.obolibrary.org/obo/OMIM_229300 CCO LOOM
http://www.limics.org/hrdo/rdfns#pat_id_45 HRDO LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_12705 NATPRO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.574.500.825.200 RH-MESH LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84718 NCIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.854.787.200 RH-MESH LOOM
http://purl.obolibrary.org/obo/MONDO_0100339 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0100339 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0100339 EFO LOOM
http://purl.obolibrary.org/obo/OGMD_0000066 OGMD LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.660.300 RH-MESH LOOM
rgo:13244 GAMUTS LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#5262 OCHV LOOM
http://purl.obolibrary.org/obo/NCIT_C84718 BERO LOOM
http://purl.bioontology.org/ontology/OMIM/229300 OMIM LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0016719 MEDLINEPLUS LOOM
http://id.nlm.nih.gov/mesh/D005621 MDM LOOM
http://radlex.org/RID/RID5152 RADLEX LOOM
http://purl.obolibrary.org/obo/OMIT_0006824 OMIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.140.252.700.150 RH-MESH LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Friedreich_Ataxia CSEO LOOM
http://purl.obolibrary.org/obo/DOID_12705 CLO LOOM
http://purl.obolibrary.org/obo/DOID_12705 DTO LOOM
http://purl.obolibrary.org/obo/DOID_12705 DOID LOOM
http://purl.obolibrary.org/obo/DOID_12705 BAO LOOM
http://purl.obolibrary.org/obo/DOID_12705 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_12705 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_12705 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_12705 FNS-H LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D005621 RH-MESH LOOM
http://purl.bioontology.org/ontology/MESH/D005621 MESH LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/10394003 SNOMEDCT LOOM
http://purl.bioontology.org/ontology/RCD/F140. RCD LOOM
http://identifiers.org/omim/229300 REXO LOOM
http://identifiers.org/omim/229300 GEXO LOOM
http://identifiers.org/omim/229300 RETO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.400.780.200 RH-MESH LOOM