Hypoplastic toenails

Symptom Information:

Symptom ID: HPO:0001800
Synonyms:
Hypoplastic toenails [OMIM:Hypoplastic toenails]
Quality:
Cross references:
OMIM: "Hypoplastic toenails" [OMIM:Hypoplastic toenails]
Is a (Direct Parents):
HPO         Aplastic/hypoplastic toenail
HPO         Small 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)
                Aplasia/Hypoplasia of the nails(HPO:0008386)
                   Small nail(HPO:0001792)
                      Hypoplastic toenails(HPO:0001800)
                   Aplastic/hypoplastic toenail(HPO:0010624)
                      Hypoplastic toenails(HPO:0001800)
                Abnormality of the toenails(HPO:0008388)
                   Aplastic/hypoplastic toenail(HPO:0010624)
                      Hypoplastic toenails(HPO:0001800)
MedDRA:
Database Frequency: 74 / 7739
Resource:

All diseases associated with this symptom:

2q31.1 microdeletion syndrome (Orphanet:251014)
ADAMS-OLIVER SYNDROME 4 (OMIM:615297)
Acrofacial dysostosis, Weyers type (Orphanet:952)
Adams-Oliver syndrome (Orphanet:974)
Amelo-onycho-hypohidrotic syndrome (Orphanet:1028)
Anonychia - microcephaly (Orphanet:1094)
Aphalangy - syndactyly - microcephaly (Orphanet:1113)
Bartsocas-Papas syndrome (Orphanet:1234)
Blepharoptosis - cleft palate - ectrodactyly - dental anomalies (Orphanet:1258)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
Brachytelephalangy - dysmorphism - Kallmann syndrome (Orphanet:1295)
Camptobrachydactyly (Orphanet:1319)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Cenani-Lenz syndrome (Orphanet:3258)
Cleft palate - large ears - small head (Orphanet:2013)
Coffin-Siris syndrome (Orphanet:1465)
Cooks syndrome (Orphanet:1487)
Costello syndrome (Orphanet:3071)
Cronkhite-Canada syndrome (Orphanet:2930)
Cryptomicrotia - brachydactyly - excess fingertip arch (Orphanet:1547)
Deafness - onychodystrophy (Orphanet:3231)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Distal monosomy 10p (Orphanet:1580)
Dubowitz syndrome (Orphanet:235)
Dyskeratosis congenita (Orphanet:1775)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Ellis Van Creveld syndrome (Orphanet:289)
Epidermolysis bullosa simplex with anodontia/hypodontia (Orphanet:2325)
FIBROCHONDROGENESIS 1 (OMIM:228520)
Familial clubfoot due to 17q23.1q23.2 microduplication (Orphanet:238578)
Fibrochondrogenesis (Orphanet:2021)
Fuhrmann syndrome (Orphanet:2854)
Guttmacher syndrome (Orphanet:2957)
HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT (OMIM:235830)
Hand-foot-genital syndrome (Orphanet:2438)
Hirschsprung disease - nail hypoplasia - dysmorphism (Orphanet:2153)
Hirschsprung disease - type D brachydactyly (Orphanet:2150)
Histidinuria - renal tubular defect (Orphanet:2158)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hypodontia - dysplasia of nails (Orphanet:2228)
Isotretinoin syndrome (Orphanet:2305)
Junctional epidermolysis bullosa, non-Herlitz type (Orphanet:89840)
KID syndrome (Orphanet:477)
Keipert syndrome (Orphanet:2662)
Léri-Weill dyschondrosteosis (Orphanet:240)
McDonough syndrome (Orphanet:2471)
Microcephaly - intellectual deficit - phalangeal and neurological anomalies (Orphanet:137658)
Monosomy 22q13 (Orphanet:48652)
Mycophenolate mofetil embryopathy (Orphanet:268249)
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)
Oculotrichodysplasia (Orphanet:2718)
Odonto-onycho dysplasia - alopecia (Orphanet:2722)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Osteoglophonic dwarfism (Orphanet:2645)
Pectus excavatum - macrocephaly - dysplastic nails (Orphanet:2835)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Schneckenbecken dysplasia (Orphanet:3144)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Severe intellectual deficit - epilepsy - anal anomalies - distal phalangeal hypoplasia (Orphanet:94066)
Taurodontia - absent teeth - sparse hair (Orphanet:2731)
Thymic-renal-anal-lung dysplasia (Orphanet:3326)
Trisomy 1q (Orphanet:261344)
Trisomy 9p (Orphanet:236)
Turner syndrome (Orphanet:881)
Ulna hypoplasia - intellectual deficit (Orphanet:2249)
Ulnar-mammary syndrome (Orphanet:3138)
Weaver syndrome (Orphanet:3447)
Williams syndrome (Orphanet:904)
Yunis-Varon syndrome (Orphanet:3472)
Zimmermann-Laband syndrome (Orphanet:3473)