Onycholysis

Symptom Information:

Symptom ID: HPO:0001806
Synonyms:
Oncholysis [HPO:0001806]
Onycholysis (disorder) [Orphanet:25650]
Lamellar nail splitting (disorder) [Orphanet:25650]
Onycholysis [Orphanet:25650]
Lamellar nail splitting [Orphanet:25650]
Oncholysis [OMIM:Oncholysis]
Onycholysis [OMIM:Onycholysis]
Onychoschisis [Orphanet:25650]
Onycholysis [MedDRA:10030337]
Onychoclasis [MedDRA:10048886]
Brittle nails [MedDRA:10048886]
Onychoschizia [MedDRA:10048886]
Onychorrhexis [MedDRA:10048886]
Onychoschisis [MedDRA:10048886]
Splitting nails [MedDRA:10048886]
Broken nails [MedDRA:10048886]
Onychorrhexis [OMIM:Onychorrhexis]
Quality:
Cross references:
Orphanet:25650 "Onycholysis" [Orphanet:25650]
OMIM: "Oncholysis" [OMIM:Oncholysis]
OMIM: "Onycholysis" [OMIM:Onycholysis]
OMIM: "Onychorrhexis" [OMIM:Onychorrhexis]
UMLS:C0085661 "Onycholysis" [HPO:0001806]
UMLS:C0085661 "Onycholysis" [Orphanet:25650]
UMLS:C0263531 "Lamellar nail splitting" [Orphanet:25650]
Is a (Direct Parents):
MedDRA Nail and nail bed conditions (excl infections and infestations)
Orphanet Abnormality of the nail
HPO         Onycholysis of fingernails
HPO         Onycholysis of toenails
HPO         Abnormality of the nail
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)
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)