Leukonychia
Symptom Information:
Symptom ID: | HPO:0001820 | |||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) |
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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) |