Abnormality of the fingernails
Symptom Information:
Symptom ID: | HPO:0001231 | ||||||||
Synonyms: |
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Quality: | |||||||||
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) Abnormality of the fingernails(HPO:0001231) MedDRA: |
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Database Frequency: | 116 / 7739 | ||||||||
Resource: |
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) |