Abnormality of the fingernails

Symptom Information:

Symptom ID: HPO:0001231
Fingernail anomaly [Orphanet:25050]
Abnormal fingernails [Orphanet:25050]
Cross references:
Orphanet:25050 "Abnormal fingernails" [Orphanet:25050]
Is a (Direct Parents):
Orphanet Abnormality of the nail
HPO         Abnormality of the nail
HPO         Thin fingernail
HPO         Onycholysis of fingernails
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the nail(HPO:0001597)
                Abnormality of the fingernails(HPO:0001231)
Database Frequency: 116 / 7739

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
AREDYLD syndrome (Orphanet:1133)
Acrocraniofacial dysostosis (Orphanet:949)
Acrofacial dysostosis, Weyers type (Orphanet:952)
Acroosteolysis, dominant type (Orphanet:955)
Allergic bronchopulmonary aspergillosis (Orphanet:1164)
Amelo-onycho-hypohidrotic syndrome (Orphanet:1028)
Aphalangy - syndactyly - microcephaly (Orphanet:1113)
Arthrogryposis multiplex congenita - whistling face (Orphanet:1150)
Autosomal dominant hypocalcemia (Orphanet:428)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
Brachydactyly - elbow wrist dysplasia (Orphanet:1275)
Brachydactyly - preaxial hallux varus (Orphanet:1278)
Brachydactyly type C (Orphanet:93384)
Brachyolmia, Maroteaux type (Orphanet:93302)
Böök syndrome (Orphanet:1262)
CHARGE syndrome (Orphanet:138)
Camptobrachydactyly (Orphanet:1319)
Central congenital hypothyroidism (Orphanet:226298)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Coloboma of macula - brachydactyly type B (Orphanet:1471)
Congenital absence/hypoplasia of fingers excluding thumb, unilateral (Orphanet:973)
Costello syndrome (Orphanet:3071)
Cranioectodermal dysplasia (Orphanet:1515)
Cronkhite-Canada syndrome (Orphanet:2930)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Distal monosomy 10p (Orphanet:1580)
Dubowitz syndrome (Orphanet:235)
Dyskeratosis congenita (Orphanet:1775)
Ectodermal dysplasia - blindness (Orphanet:1806)
Ellis Van Creveld syndrome (Orphanet:289)
Epidermolysis bullosa simplex (Orphanet:304)
Epidermolysis bullosa simplex with anodontia/hypodontia (Orphanet:2325)
Epidermolysis bullosa simplex with mottled pigmentation (Orphanet:79397)
Epidermolysis bullosa simplex with muscular dystrophy (Orphanet:257)
Epidermolysis bullosa simplex, Dowling-Meara type (Orphanet:79396)
Epidermolytic palmoplantar keratoderma (Orphanet:2199)
Fine-Lubinsky syndrome (Orphanet:1272)
Floating-Harbor syndrome (Orphanet:2044)
Fuhrmann syndrome (Orphanet:2854)
Fukuda-Miyanomae-Nakata syndrome (Orphanet:2060)
Generalized dominant dystrophic epidermolysis bullosa (Orphanet:231568)
Generalized junctional epidermolysis bullosa, non-Herlitz type (Orphanet:79402)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hirschsprung disease - nail hypoplasia - dysmorphism (Orphanet:2153)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hydrocephalus - blue sclerae - nephropathy (Orphanet:2186)
Hypoglossia - hypodactyly (Orphanet:989)
Hypospadias - intellectual deficit, Goldblatt type (Orphanet:2261)
Ichthyosis - intellectual deficit - dwarfism - renal impairment (Orphanet:2278)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Ichthyosis hystrix of Curth-Macklin (Orphanet:79503)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Junctional epidermolysis bullosa inversa (Orphanet:79405)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)
KID syndrome (Orphanet:477)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
LOC syndrome (Orphanet:2407)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Leukonychia totalis (Orphanet:2387)
Lichen planopilaris (Orphanet:525)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Mononen-Karnes-Senac syndrome (Orphanet:2565)
Monosomy 9p (Orphanet:261112)
Mosaic trisomy 9 (Orphanet:99776)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Nail-patella syndrome (Orphanet:2614)
Non-distal trisomy 13q (Orphanet:1702)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Oculodentodigital dysplasia (Orphanet:2710)
Oculotrichodysplasia (Orphanet:2718)
Odonto-onycho dysplasia - alopecia (Orphanet:2722)
Odontomicronychial dysplasia (Orphanet:1811)
Odontotrichomelic syndrome (Orphanet:2723)
Okamoto syndrome (Orphanet:2729)
Orofaciodigital syndrome type 3 (Orphanet:2752)
Osteocraniostenosis (Orphanet:2763)
Pachydermoperiostosis (Orphanet:2796)
Pachyonychia congenita (Orphanet:2309)
Palmoplantar keratoderma-spastic paralysis syndrome (Orphanet:2201)
Papillon-Lefèvre syndrome (Orphanet:678)
Phocomelia, Schinzel type (Orphanet:2879)
Pierre Robin syndrome - faciodigital anomaly (Orphanet:2888)
Pretibial dystrophic epidermolysis bullosa (Orphanet:79410)
Prolidase deficiency (Orphanet:742)
Rabson-Mendenhall syndrome (Orphanet:769)
Recessive dystrophic epidermolysis bullosa-generalized other (Orphanet:89842)
Rothmund-Thomson syndrome (Orphanet:2909)
Scalp-ear-nipple syndrome (Orphanet:2036)
Schinzel-Giedion syndrome (Orphanet:798)
Schneckenbecken dysplasia (Orphanet:3144)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Sotos syndrome (Orphanet:821)
Stern-Lubinsky-Durrie syndrome (Orphanet:3194)
Taurodontia - absent teeth - sparse hair (Orphanet:2731)
Thymic-renal-anal-lung dysplasia (Orphanet:3326)
Transgrediens et progrediens palmoplantar keratoderma (Orphanet:495)
Tricho-dento-osseous syndrome (Orphanet:3352)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Trigonocephaly - broad thumbs (Orphanet:3365)
Trisomy 1q (Orphanet:261344)
Turner syndrome (Orphanet:881)
Ulnar-mammary syndrome (Orphanet:3138)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Weaver syndrome (Orphanet:3447)
Williams syndrome (Orphanet:904)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)
Yellow nail syndrome (Orphanet:662)
Zimmermann-Laband syndrome (Orphanet:3473)