ORPHA:207021

Rare hereditary systemic disease with peripheral neuropathy

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	Rare hereditary systemic disease with peripheral neuropathy
fr	Maladie systémique héréditaire avec neuropathie périphérique
de	Seltene hereditäre systemische Krankheit mit peripherer Neuropathie
es	Enfermedad sistémica rara hereditaria con neuropatía periférica
it	Malattia sistemica ereditaria rara con neuropatia periferica
nl	Zeldzame erfelijke systemische ziekte met perifere neuropathie
pt	Doença rara hereditária sistémica com neuropatia periférica
pl	Rzadka dziedziczna choroba układowa z neuropatią obwodową
cs	Vzácná hereditární systémová onemocnění s periferní neuropatií
uk	Рідкісне спадкове системне захворювання з периферичною нейропатією
zh	罕见遗传性系统性疾病伴周围神经病
tr	Periferik nöropati ile seyreden nadir kalıtsal sistemik hastalık

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	16134	E		validated
UMLS	C5680813	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:207015Rare hereditary disease with peripheral 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/207021
This record as JSON: /data/d/207021.json