ORPHA:307711

Disease with diffuse palmoplantar keratoderma as a major feature

Synonyms: Disease with diffuse palmoplantar hyperkeratosis as a major feature

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	Disease with diffuse palmoplantar keratoderma as a major feature	Disease with diffuse palmoplantar hyperkeratosis as a major feature
fr	Maladie avec une kératodermie palmoplantaire diffuse comme manifestation majeure	Maladie avec une hyperkératose palmoplantaire diffuse comme manifestation majeure
de	Krankheit mit diffuser Palmoplantarkeratose als Hauptmerkmal
es	Enfermedad con queratodermia palmoplantar difusa como característica principal	Enfermedad con hiperqueratosis palmoplantar difusa como característica principal
it	Malattia con cheratoderma palmoplantare diffuso come segno cardinale	Malattia con ipercheratosi palmoplantare diffusa come segno cardinale
nl	Ziekte met diffuse palmoplantaire keratodermie als hoofdkenmerk	Ziekte met diffuse palmoplantaire hyperkeratose als hoofdkenmerk
pt	Doença com queratodermia palmoplantar difusa como característica principal
pl	Choroba z rozlanym rogowcem dłoniowo-podeszwowym jako objawem głównym	Choroba z rozlaną hiperkeratozą dłoniowo-podeszwową jako objawem głównym
cs	Onemocnění s difuzní palmoplantární keratodermou jako hlavním příznakem	Onemocnění s difuzní palmoplantární hyperkeratózou jako hlavním příznakem
uk	Захворювання з дифузною долонно-підошовною кератодермією як основною ознакою	Захворювання з дифузним долонно-підошовним гіперкератозом як основною ознакою
zh	弥漫性掌跖角化症为主要特征的疾病	弥漫性掌跖角化症为主要特征疾病
tr	Esas klinik özelliği yaygın palmoplantar keratoderma olan hastalık	Esas klinik özelliği yaygın palmoplantar hiperkeratoz olan hastalık

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	17669	E		validated
UMLS	C5679958	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:89826Rare skin disease

Parents in the classifications (1):

ORPHA:307141Diffuse palmoplantar keratoderma
rare genetic diseases; rare skin diseases

Children (2):

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/307711
This record as JSON: /data/d/307711.json