Leukonychia

Symptom Information:

Symptom ID: HPO:0001820
Synonyms:
Leukonychia (disorder) [Orphanet:25600]
Leuconychia [HPO:0001820]
Leukonychia [Orphanet:25600]
Leukonychia [OMIM:Leukonychia]
Abnormal nails colour/leukonychia/melanonychia [Orphanet:25600]
Nail discolouration [MedDRA:10028692]
Discoloration nail [MedDRA:10028692]
Nail discoloration [MedDRA:10028692]
Fingernail discoloration [MedDRA:10028692]
Leukonychia [MedDRA:10028692]
Discolouration nail [MedDRA:10028692]
Fingernail discolouration [MedDRA:10028692]
Toenail discoloration [MedDRA:10028692]
Toenail discolouration [MedDRA:10028692]
Leukonychia (rare) [OMIM:Leukonychia (rare)]
Quality:
Cross references:
Orphanet:25600 "Abnormal nails colour/leukonychia/melanonychia" [Orphanet:25600]
OMIM: "Leukonychia" [OMIM:Leukonychia]
OMIM: "Leukonychia (rare)" [OMIM:Leukonychia (rare)]
UMLS:C0240182 "Leuconychia" [HPO:0001820]
UMLS:C0240182 "Leukonychia" [Orphanet:25600]
Is a (Direct Parents):
MedDRA Nail and nail bed conditions (excl infections and infestations)
Orphanet Abnormality of the nail
HPO         Abnormality of nail color
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the nail(HPO:0001597)
                Abnormality of nail color(HPO:0100643)
                   Leukonychia(HPO:0001820)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin appendage conditions(MedDRA:10040798)
       Nail and nail bed conditions (excl infections and infestations)(MedDRA:10028685)
          Leukonychia(HPO:0001820)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Atrophoderma vermiculata (Orphanet:79100)
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis (OMIM:615821)
Cronkhite-Canada syndrome (Orphanet:2930)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Ectodermal dysplasia syndrome (Orphanet:79373)
HOOFT DISEASE (OMIM:236300)
Hidrotic ectodermal dysplasia (Orphanet:189)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A (OMIM:601277)
Kawasaki disease (Orphanet:2331)
Knuckle pads-leuconychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome (Orphanet:2698)
Leukonychia totalis (Orphanet:2387)
Lowry-Wood syndrome (Orphanet:1824)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Pachyonychia congenita (Orphanet:2309)
Peutz-Jeghers syndrome (Orphanet:2869)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Yellow nail syndrome (Orphanet:662)