Abnormality of the nail

Symptom Information:

Symptom ID: HPO:0001597
Synonyms:
Nail disease [HPO:0001597]
Nail anomaly [Orphanet:25000]
Congenital anomaly of nail (disorder) [Orphanet:25000]
Congenital anomaly of nail [Orphanet:25000]
Nails anomalies [Orphanet:25000]
Nail anomalies [OMIM:Nail anomalies]
Quality:
Cross references:
Orphanet:25000 "Nails anomalies" [Orphanet:25000]
OMIM: "Nail anomalies" [OMIM:Nail anomalies]
UMLS:C0265997 "Congenital anomaly of nail" [Orphanet:25000]
Is a (Direct Parents):
HPO         Abnormality of skin adnexa
HPO         Nail bed hemorrhage
HPO         Ingrown 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)
MedDRA:
Database Frequency: 115 / 7739
Resource:

All diseases associated with this symptom:

ADULT syndrome (Orphanet:978)
Acquired epidermolysis bullosa (Orphanet:46487)
Acral dystrophic epidermolysis bullosa (Orphanet:158673)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Acrodysostosis (Orphanet:950)
Acrokeratoelastoidosis of Costa (Orphanet:38)
Acromelanosis (Orphanet:39)
Alkaptonuria (Orphanet:56)
Autosomal dominant hypocalcemia (Orphanet:428)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
Autosomal recessive epidermolysis bullosa simplex (Orphanet:89838)
Bullous dystrophy, macular type (Orphanet:1867)
CANDIDIASIS, FAMILIAL, 2 (OMIM:212050)
CHILD syndrome (Orphanet:139)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Chilblain lupus (Orphanet:90280)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Classical mycosis fungoides (Orphanet:2584)
Congenital absence/hypoplasia of fingers excluding thumb (Orphanet:294990)
Congenital non-bullous ichthyosiform erythroderma (Orphanet:79394)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Darier disease (Orphanet:218)
Dermatomyositis (Orphanet:221)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Dystrophic epidermolysis bullosa (Orphanet:303)
Dystrophic epidermolysis bullosa pruriginosa (Orphanet:89843)
Dystrophic epidermolysis bullosa, nails only (Orphanet:158676)
ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET (OMIM:129540)
Ectodermal dysplasia with natal teeth, Turnpenny type (Orphanet:69083)
Ellis Van Creveld syndrome (Orphanet:289)
Epidermolysis bullosa simplex (Orphanet:304)
Epidermolysis bullosa simplex due to plakophilin deficiency (Orphanet:158668)
Epidermolysis bullosa simplex superficialis (Orphanet:89839)
Epidermolysis bullosa simplex with mottled pigmentation (Orphanet:79397)
Epidermolysis bullosa simplex, Dowling-Meara type (Orphanet:79396)
Epidermolysis bullosa simplex, Ogna type (Orphanet:79401)
Erythrokeratodermia variabilis (Orphanet:317)
FLOTCH syndrome (Orphanet:2045)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Focal dermal hypoplasia (Orphanet:2092)
Focal palmoplantar and gingival keratoderma (Orphanet:2200)
Fucosidosis (Orphanet:349)
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type (Orphanet:79399)
Generalized junctional epidermolysis bullosa, non-Herlitz type (Orphanet:79402)
Growth hormone insensitivity syndrome (Orphanet:181393)
Hereditary painful callosities (Orphanet:79141)
Hidrotic ectodermal dysplasia, Christianson-Fourie type (Orphanet:1808)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hypodontia - dysplasia of nails (Orphanet:2228)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
Hypospadias - intellectual deficit, Goldblatt type (Orphanet:2261)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Hypotrichosis with juvenile macular degeneration (Orphanet:1573)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Ichthyosis-hypotrichosis syndrome (Orphanet:91132)
Incontinentia pigmenti (Orphanet:464)
Inherited epidermolysis bullosa (Orphanet:79361)
Intellectual deficit, Wolff type (Orphanet:3080)
Isolated punctate palmoplantar keratoderma (Orphanet:2338)
Johanson-Blizzard syndrome (Orphanet:2315)
Junctional epidermolysis bullosa - pyloric atresia (Orphanet:79403)
Junctional epidermolysis bullosa, non-Herlitz type (Orphanet:89840)
Juvenile idiopathic arthritis (Orphanet:92)
Keipert syndrome (Orphanet:2662)
Keratoderma hereditarium mutilans (Orphanet:494)
Keratoderma hereditarium mutilans with ichthyosis (Orphanet:79395)
Keratosis palmoplantaris striata (Orphanet:50942)
LUNULAE OF FINGERNAILS (OMIM:152600)
Lamellar ichthyosis (Orphanet:313)
Lowry-MacLean syndrome (Orphanet:2409)
Lymphedema - atrial septal defects - facial changes (Orphanet:86915)
Mal de Meleda (Orphanet:87503)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Milroy disease (Orphanet:79452)
Moebius syndrome (Orphanet:570)
Monilethrix (Orphanet:573)
Multiple synostoses syndrome (Orphanet:3237)
NAIL HIGH-SULFUR PROTEIN (OMIM:161070)
NAIL LOW-SULFUR PROTEIN (OMIM:161080)
NAILBEDS, PIGMENTATION OF (OMIM:161100)
OTOONYCHOPERONEAL SYNDROME (OMIM:259780)
Oculodentodigital dysplasia (Orphanet:2710)
Odontomicronychial dysplasia (Orphanet:1811)
Oto-onycho-peroneal syndrome (Orphanet:2793)
Pachyonychia congenita (Orphanet:2309)
Palmoplantar keratoderma-sclerodactyly syndrome (Orphanet:384)
Papillon-Lefèvre syndrome (Orphanet:678)
Pili torti (Orphanet:2889)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Pityriasis rubra pilaris (Orphanet:2897)
Primary cutaneous lymphoma (Orphanet:542)
Progeroid syndrome, Petty type (Orphanet:2963)
Proteus syndrome (Orphanet:744)
Pseudo-pelade of Brocq (Orphanet:129)
Punctate palmoplantar keratoderma type 1 (Orphanet:79501)
Pycnodysostosis (Orphanet:763)
Reactive arthritis (Orphanet:29207)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)
Rothmund-Thomson syndrome (Orphanet:2909)
Rothmund-Thomson syndrome type 1 (Orphanet:221008)
Rothmund-Thomson syndrome type 2 (Orphanet:221016)
Schöpf-Schulz-Passarge syndrome (Orphanet:50944)
Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy (Orphanet:169095)
Split hand - split foot - deafness (Orphanet:71271)
Spondylometaphyseal dysplasia, Golden type (Orphanet:168544)
Steatocystoma multiplex - natal teeth (Orphanet:3184)
Sézary syndrome (Orphanet:3162)
TOE, ROTATED FIFTH (OMIM:189150)
Transient bullous dermolysis of the newborn (Orphanet:79411)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Tyrosinemia type 2 (Orphanet:28378)
Woolly hair - hypotrichosis - everted lower lip - outstanding ears (Orphanet:1409)