Hypoplastic fingernail

Symptom Information:

Symptom ID: HPO:0001804
Hypoplastic fingernails [OMIM:Hypoplastic fingernails]
Cross references:
OMIM: "Hypoplastic fingernails" [OMIM:Hypoplastic fingernails]
Is a (Direct Parents):
HPO         Small nail
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)
                Aplasia/Hypoplasia of the nails(HPO:0008386)
                   Small nail(HPO:0001792)
                      Hypoplastic fingernail(HPO:0001804)
Database Frequency: 62 / 7739

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
Acrocapitofemoral dysplasia (Orphanet:63446)
Adams-Oliver syndrome (Orphanet:974)
Anonychia - microcephaly (Orphanet:1094)
Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis (Orphanet:1112)
Aphalangy - syndactyly - microcephaly (Orphanet:1113)
Autosomal dominant Larsen syndrome (Orphanet:503)
Brachydactyly type B (Orphanet:93383)
Brachydactyly type B2 (Orphanet:140908)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
Branchio-oculo-facial syndrome (Orphanet:1297)
Cenani-Lenz syndrome (Orphanet:3258)
Coffin-Lowry syndrome (Orphanet:192)
Coffin-Siris syndrome (Orphanet:1465)
Coloboma of macula - brachydactyly type B (Orphanet:1471)
Cooks syndrome (Orphanet:1487)
Dahlberg-Borer-Newcomer syndrome (Orphanet:1563)
Deafness - onychodystrophy (Orphanet:3231)
Diaphanospondylodysostosis (Orphanet:66637)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Dyskeratosis congenita (Orphanet:1775)
Dystrophic epidermolysis bullosa (Orphanet:303)
Embryofetopathy due to oral anticoagulant therapy (Orphanet:1914)
Epidermolysis bullosa simplex (Orphanet:304)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Familial visceral myopathy (Orphanet:2604)
Fetal hydantoin syndrome (Orphanet:1912)
Fibrochondrogenesis (Orphanet:2021)
Fryns syndrome (Orphanet:2059)
Fuhrmann syndrome (Orphanet:2854)
Greenberg dysplasia (Orphanet:1426)
Hirschsprung disease - type D brachydactyly (Orphanet:2150)
Hypodontia - dysplasia of nails (Orphanet:2228)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Junctional epidermolysis bullosa, non-Herlitz type (Orphanet:89840)
Keipert syndrome (Orphanet:2662)
LOC syndrome (Orphanet:2407)
Lethal acantholytic epidermolysis bullosa (Orphanet:158687)
Léri-Weill dyschondrosteosis (Orphanet:240)
Melhem-Fahl syndrome (Orphanet:2482)
Multiple epiphyseal dysplasia (Orphanet:251)
Multiple epiphyseal dysplasia, Beighton type (Orphanet:166011)
Nail-patella syndrome (Orphanet:2614)
Odontotrichomelic syndrome (Orphanet:2723)
Orofaciodigital syndrome type 10 (Orphanet:2756)
Otopalatodigital syndrome (Orphanet:669)
Pachyonychia congenita (Orphanet:2309)
Progeroid syndrome, Petty type (Orphanet:2963)
Pycnodysostosis (Orphanet:763)
Rudiger syndrome (Orphanet:3118)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Sillence syndrome (Orphanet:3168)
Stern-Lubinsky-Durrie syndrome (Orphanet:3194)
Toluene embryopathy (Orphanet:1920)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Ulna hypoplasia - intellectual deficit (Orphanet:2249)
Yunis-Varon syndrome (Orphanet:3472)
Zimmermann-Laband syndrome (Orphanet:3473)