Hypoplastic toenails
Symptom Information:
Symptom ID: | HPO:0001800 | ||||
Synonyms: |
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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) 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: |
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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) |