Thick nail

Symptom Information:

Symptom ID: HPO:0001805
Dystrophic thickened nails [HPO:0001805]
Onychogryposis [HPO:0001805]
Thickened nails [HPO:0001805]
Thick nail of hand [Orphanet:25200]
Thick nail of foot [Orphanet:25450]
Onychogryphosis [HPO:0001805]
Dystrophic thickened nails [OMIM:Dystrophic thickened nails]
Onychogryposis [OMIM:Onychogryposis]
Thickened nails [OMIM:Thickened nails]
Dysplastic/thick/grooved fingernails [Orphanet:25200]
Dysplastic/thick/grooved toenails [Orphanet:25450]
Thick nails (in some patients) [OMIM:Thick nails (in some patients)]
Thickened nails (in some patients) [OMIM:Thickened nails (in some patients)]
Onychogryphosis [MedDRA:10030336]
Cross references:
Orphanet:25200 "Dysplastic/thick/grooved fingernails" [Orphanet:25200]
Orphanet:25450 "Dysplastic/thick/grooved toenails" [Orphanet:25450]
OMIM: "Dystrophic thickened nails" [OMIM:Dystrophic thickened nails]
OMIM: "Onychogryposis" [OMIM:Onychogryposis]
OMIM: "Thickened nails" [OMIM:Thickened nails]
OMIM: "Thick nails (in some patients)" [OMIM:Thick nails (in some patients)]
OMIM: "Thickened nails (in some patients)" [OMIM:Thickened nails (in some patients)]
UMLS:C0263537 "Onychogryphosis" [HPO:0001805]
Is a (Direct Parents):
HPO         Onychogryposis of fingernail
Orphanet Abnormality of the fingernails
Orphanet Abnormality of the toenails
HPO         Nail dystrophy
MedDRA Nail and nail bed conditions (excl infections and infestations)
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)
                Nail dystrophy(HPO:0008404)
                   Thick nail(HPO:0001805)
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin appendage conditions(MedDRA:10040798)
       Nail and nail bed conditions (excl infections and infestations)(MedDRA:10028685)
          Thick nail(HPO:0001805)
Database Frequency: 96 / 7739

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
ADULT syndrome (Orphanet:978)
Ackerman syndrome (Orphanet:2561)
Acro-oto-ocular syndrome (Orphanet:2980)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Acrofacial dysostosis, Weyers type (Orphanet:952)
Acromegaly (Orphanet:963)
Acromelic frontonasal dysplasia (Orphanet:1827)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Aminopterin/methotrexate embryofetopathy (Orphanet:1908)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Antecubital pterygium syndrome (Orphanet:2987)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal dominant nail dysplasia (Orphanet:79153)
Autosomal dominant palmoplantar keratoderma and congenital alopecia (Orphanet:1010)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive epidermolysis bullosa simplex (Orphanet:89838)
Autosomal recessive palmoplantar keratoderma and congenital alopecia (Orphanet:1366)
Blepharoptosis - myopia - ectopia lentis (Orphanet:1259)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
Brain malformation - congenital heart disease - postaxial polydactyly (Orphanet:75389)
Branchio-oculo-facial syndrome (Orphanet:1297)
CHILD syndrome (Orphanet:139)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Charlie M syndrome (Orphanet:1406)
Choroidal atrophy - alopecia (Orphanet:1433)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Congenital cataract - ichthyosis (Orphanet:1376)
Cooks syndrome (Orphanet:1487)
Cranioectodermal dysplasia 4 (OMIM:614378)
Craniofrontonasal dysplasia (Orphanet:1520)
Cronkhite-Canada syndrome (Orphanet:2930)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Dermo-odonto dysplasia (Orphanet:1660)
Dyskeratosis congenita (Orphanet:1775)
Dystrophic epidermolysis bullosa (Orphanet:303)
EEC syndrome (Orphanet:1896)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ectodermal dysplasia, tricho-odonto-onychial type (Orphanet:1818)
Epidermolysis bullosa simplex with anodontia/hypodontia (Orphanet:2325)
Epidermolysis bullosa simplex with mottled pigmentation (Orphanet:79397)
Fine-Lubinsky syndrome (Orphanet:1272)
Focal palmoplantar and gingival keratoderma (Orphanet:2200)
Gómez-López-Hernández syndrome (Orphanet:1532)
Haim-Munk syndrome (Orphanet:2342)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hereditary sensory and autonomic neuropathy type 2 (Orphanet:970)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hidrotic ectodermal dysplasia, Christianson-Fourie type (Orphanet:1808)
Hidrotic ectodermal dysplasia, Halal type (Orphanet:1809)
Hypodontia - dysplasia of nails (Orphanet:2228)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit (Orphanet:2269)
Incontinentia pigmenti (Orphanet:464)
Junctional epidermolysis bullosa (Orphanet:305)
Juvenile idiopathic arthritis (Orphanet:92)
KID syndrome (Orphanet:477)
Keratoderma hereditarium mutilans (Orphanet:494)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Naegeli-Franceschetti-Jadassohn syndrome (Orphanet:69087)
Nail-patella syndrome (Orphanet:2614)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
Neonatal inflammatory skin and bowel disease (Orphanet:294023)
Oculo-skeletal-renal syndrome (Orphanet:2716)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Omenn syndrome (Orphanet:39041)
Oro-mandibular-limb hypogenesis syndrome (Orphanet:2749)
Pachyonychia congenita (Orphanet:2309)
Pallister-Hall syndrome (Orphanet:672)
Papillon-Lefèvre syndrome (Orphanet:678)
Paraplegia - intellectual deficit - hyperkeratosis (Orphanet:2824)
Pectus excavatum - macrocephaly - dysplastic nails (Orphanet:2835)
Pili torti - onychodysplasia (Orphanet:2890)
Pityriasis rubra pilaris (Orphanet:2897)
Pycnodysostosis (Orphanet:763)
Rabson-Mendenhall syndrome (Orphanet:769)
Reactive arthritis (Orphanet:29207)
Sclerosteosis (Orphanet:3152)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
Stoll-Alembik-Finck syndrome (Orphanet:3200)
Thumb deformity - alopecia - pigmentation anomaly (Orphanet:2251)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Tricho-odonto-onychial dysplasia (Orphanet:3355)
Trisomy 9p (Orphanet:236)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
Yellow nail syndrome (Orphanet:662)
Zimmermann-Laband syndrome (Orphanet:3473)
Zlotogora-Ogur syndrome (Orphanet:3253)