Fragile nails
Symptom Information:
Symptom ID: | HPO:0001808 | ||||||||||||||
Synonyms: |
|
||||||||||||||
Quality: | |||||||||||||||
Cross references: |
|
||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||
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) Fragile nails(HPO:0001808) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Pilar disorders NEC(MedDRA:10035035) Fragile nails(HPO:0001808) |
||||||||||||||
Database Frequency: | 21 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
Argininosuccinic aciduria | (Orphanet:23) |
Beckwith-Wiedemann syndrome due to NSD1 mutation | (Orphanet:238613) |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis | (OMIM:615821) |
Costello syndrome | (Orphanet:3071) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE | (OMIM:602032) |
Generalized junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:79402) |
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS | (OMIM:242150) |
Junctional epidermolysis bullosa inversa | (Orphanet:79405) |
Junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:89840) |
Langer-Giedion syndrome | (Orphanet:502) |
Localized junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:251393) |
Mal de Meleda | (Orphanet:87503) |
Naegeli-Franceschetti-Jadassohn syndrome | (Orphanet:69087) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Oculotrichodysplasia | (Orphanet:2718) |
Renal tubulopathy - encephalopathy - liver failure | (Orphanet:254902) |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE | (OMIM:601675) |
Tricho-dento-osseous syndrome | (Orphanet:3352) |
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome | (Orphanet:65282) |
Wrinkly skin syndrome | (Orphanet:2834) |