Hypoplastic fingernail
Symptom Information:
| Symptom ID: | HPO:0001804 | ||
| 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) Aplasia/Hypoplasia of the nails(HPO:0008386) Small nail(HPO:0001792) Hypoplastic fingernail(HPO:0001804) MedDRA: |
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| Database Frequency: | 62 / 7739 | ||
| Resource: |
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) |
| FIBROCHONDROGENESIS 1 | (OMIM:228520) |
| 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) |
| ONYCHOTRICHODYSPLASIA AND NEUTROPENIA | (OMIM:258360) |
| 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) |