Oral leukoplakia

Symptom Information:

Symptom ID: HPO:0002745
Synonyms:
leukokeratosis [HPO:0002745]
Leukoplakia [Orphanet:23370]
Leukoplakia [HPO:0002745]
Leukoplakia (morphologic abnormality) [Orphanet:23370]
Leukokeratosis (morphologic abnormality) [Orphanet:23370]
Leukoplakia (disorder) [Orphanet:23370]
Leukokeratosis [Orphanet:23370]
Oral leukoplakia [OMIM:Oral leukoplakia]
Enanthema/aphtosa/aphta/leukoplakia [Orphanet:23370]
Leukoplakia [MedDRA:10062037]
Hairy leukoplakia (exc oral) [MedDRA:10062037]
Leukoplakia (exc anogenital) [MedDRA:10062037]
Leukoplakia NOS [MedDRA:10062037]
Leukoplakia (excl anogenital) [MedDRA:10062037]
Leukoplakia [OMIM:Leukoplakia]
Leukoplakia (71% male patients) [OMIM:Leukoplakia (71% male patients)]
Leukoplakia (classic feature) [OMIM:Leukoplakia (classic feature)]
Leukoplakia (in some patients) [OMIM:Leukoplakia (in some patients)]
Leukoplakia (seen in recessive form) [OMIM:Leukoplakia (seen in recessive form)]
Leukoplakia (tongue) [OMIM:Leukoplakia (tongue)]
Oral leukoplakia (in some patients) [OMIM:Oral leukoplakia (in some patients)]
Aphta [Orphanet:23370]
Enanthema [MedDRA:10014579]
Mucous membrane eruption (morphologic abnormality) [Orphanet:23370]
Mucous membrane eruption [Orphanet:23370]
Leukoplakia oral [MedDRA:10024396]
Quality:
Cross references:
Orphanet:23370 "Enanthema/aphtosa/aphta/leukoplakia" [Orphanet:23370]
OMIM: "Oral leukoplakia" [OMIM:Oral leukoplakia]
OMIM: "Leukoplakia" [OMIM:Leukoplakia]
OMIM: "Leukoplakia (71% male patients)" [OMIM:Leukoplakia (71% male patients)]
OMIM: "Leukoplakia (classic feature)" [OMIM:Leukoplakia (classic feature)]
OMIM: "Leukoplakia (in some patients)" [OMIM:Leukoplakia (in some patients)]
OMIM: "Leukoplakia (seen in recessive form)" [OMIM:Leukoplakia (seen in recessive form)]
OMIM: "Leukoplakia (tongue)" [OMIM:Leukoplakia (tongue)]
OMIM: "Oral leukoplakia (in some patients)" [OMIM:Oral leukoplakia (in some patients)]
UMLS:C1704317 "Leukokeratosis" [Orphanet:23370]
UMLS:C0023531 "Leukoplakia" [Orphanet:23370]
UMLS:C0014034 "Mucous membrane eruption" [Orphanet:23370]
Is a (Direct Parents):
Orphanet Abnormality of the skin
MedDRA Skin preneoplastic conditions NEC
MedDRA Oral soft tissue disorders NEC
HPO         Abnormality of oral mucosa
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of oral mucosa(HPO:0011830)
                         Oral leukoplakia(HPO:0002745)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Cornification and dystrophic skin disorders(MedDRA:10011063)
       Skin preneoplastic conditions NEC(MedDRA:10052567)
          Oral leukoplakia(HPO:0002745)
Gastrointestinal disorders(MedDRA:10017947)
    Oral soft tissue conditions(MedDRA:10031013)
       Oral soft tissue disorders NEC(MedDRA:10031015)
          Oral leukoplakia(HPO:0002745)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

Coats plus syndrome (Orphanet:313838)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 (OMIM:127550)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 (OMIM:613989)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 (OMIM:613990)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 (OMIM:224230)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2 (OMIM:613987)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3 (OMIM:613988)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 5 (OMIM:615190)
Dyskeratosis congenita (Orphanet:1775)
Hereditary benign intraepithelial dyskeratosis (Orphanet:352657)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT (OMIM:148210)
KID syndrome (Orphanet:477)
PACHYONYCHIA CONGENITA 3 (OMIM:615726)
Pachyonychia congenita (Orphanet:2309)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)
White sponge nevus (Orphanet:171723)