Onycholysis
Symptom Information:
Symptom ID: | HPO:0001806 | |||||||||||||||||
Synonyms: |
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Cross references: |
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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) Onycholysis(HPO:0001806) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Nail and nail bed conditions (excl infections and infestations)(MedDRA:10028685) Onycholysis(HPO:0001806) |
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Database Frequency: | 20 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
Amelo-onycho-hypohidrotic syndrome | (Orphanet:1028) |
Autosomal recessive nail dysplasia | (Orphanet:280654) |
CHILD syndrome | (Orphanet:139) |
ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE | (OMIM:602032) |
ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE | (OMIM:614929) |
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:275000) |
Generalized peeling skin syndrome | (Orphanet:263543) |
Hepatoerythropoietic porphyria | (Orphanet:95159) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Junctional epidermolysis bullosa | (Orphanet:305) |
Junctional epidermolysis bullosa, Herlitz type | (Orphanet:79404) |
Lichen planopilaris | (Orphanet:525) |
Naxos disease | (Orphanet:34217) |
Nephronophthisis 2 | (OMIM:602088) |
ONYCHOTRICHODYSPLASIA AND NEUTROPENIA | (OMIM:258360) |
PSORIASIS 1, SUSCEPTIBILITY TO | (OMIM:177900) |
Pure hair and nail ectodermal dysplasia | (Orphanet:69084) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
Singleton-Merten dysplasia | (Orphanet:85191) |
Stern-Lubinsky-Durrie syndrome | (Orphanet:3194) |