ORPHA:401993

Cold-induced sweating syndrome-hyperthermia spectrum

Type: Clinical group
Group: Group of disorders
Inheritance: Autosomal recessive
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	Cold-induced sweating syndrome-hyperthermia spectrum
fr	Spectre transpiration induite par le froid-hyperthermie
de	Kälteinduziertes Schwitzen-Hyperthermie-Spektrum
es	Espectro del síndrome de sudoración-hipertermia inducido por el frío
it	Spettro sindrome da sudorazione indotta dal freddo-ipertermia
nl	Koudegeïnduceerd zweten-syndroom - hyperthermie-spectrum
pt	Espectro clínico de síndrome de sudorese induzida pelo frio-hipertermia
pl	Zespół potliwości indukowany zimnem-spekrum hipertermii
cs	Spektrum zahrnující chladem indukovaný syndrom nadměrného pocení a hypertermii
uk	Спектр синдрому холодового потовиділення-гіпертермії
zh	冷诱发出汗综合征-发热症候群
tr	Soğuktan kaynaklanan terleme sendromu-hipertermi spektrumu

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	Validation
MONDO	0018431	E	validated
MONDO	18431	E	validated
UMLS	C5681139	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 (1):

ORPHA:140477Autosomal recessive hereditary sensory and autonomic neuropathy
rare genetic diseases; rare neurological diseases

Children (4):

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/401993
This record as JSON: /data/d/401993.json