ORPHA:306708

Frontotemporal neurodegeneration with movement disorder

Type: Category
Group: Group of disorders
Status: active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Frontotemporal neurodegeneration with movement disorder
fr	Neurodégénérescence frontotemporale avec trouble du mouvement
de	Frontotemporale Neurodegeneration mit Bewegungsstörung
es	Neurodegeneración frontotemporal con trastorno del movimiento
it	Neurodegenerazione frontotemporale con disturbo del movimento
nl	Frontotemporale neurodegeneratie met bewegingsstoornis
pt	Neurodegenerescência frontotemporal com alteração do movimento
pl	Neurodegeneracja czołowo-skroniowa z zaburzeniami ruchu
cs	Frontotemporální neurodegenerace s poruchou hybnosti
uk	Лобно-скронева нейродегенерація з руховими розладами
zh	额颞叶神经退行性变性伴运动障碍
tr	Hareket bozukluğu ile seyreden frontotemporal nörodejenerasyon

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	17643	E		validated
UMLS	C5681061	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:98006Rare neurologic disease

Parents in the classifications (2):

ORPHA:307058Miscellaneous movement disorder due to genetic neurodegenerative disease
rare genetic diseases
ORPHA:306695Miscellaneous movement disorder due to neurodegenerative disease
rare neurological diseases

Children (5):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/306708
This record as JSON: /data/d/306708.json