Abnormality of the toenails
Symptom Information:
Symptom ID: | HPO:0008388 | ||||||||
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) Abnormality of the toenails(HPO:0008388) MedDRA: |
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Database Frequency: | 28 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Acrocraniofacial dysostosis | (Orphanet:949) |
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Chronic mucocutaneous candidiasis | (Orphanet:1334) |
Cooks syndrome | (Orphanet:1487) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Deafness - enamel hypoplasia - nail defects | (Orphanet:3220) |
Dystrophic epidermolysis bullosa, nails only | (Orphanet:158676) |
Generalized dominant dystrophic epidermolysis bullosa | (Orphanet:231568) |
Generalized junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:79402) |
Hereditary orotic aciduria | (Orphanet:30) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Hypospadias - intellectual deficit, Goldblatt type | (Orphanet:2261) |
Incontinentia pigmenti | (Orphanet:464) |
Kindler syndrome | (Orphanet:2908) |
LOC syndrome | (Orphanet:2407) |
Leukonychia totalis | (Orphanet:2387) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Odontotrichomelic syndrome | (Orphanet:2723) |
Palmoplantar keratoderma-spastic paralysis syndrome | (Orphanet:2201) |
Pretibial dystrophic epidermolysis bullosa | (Orphanet:79410) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Trigonocephaly - broad thumbs | (Orphanet:3365) |
Trisomy 18 | (Orphanet:3380) |
Yellow nail syndrome | (Orphanet:662) |