Short nail
Symptom Information:
Symptom ID: | HPO:0001799 | ||
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) Short nail(HPO:0001799) MedDRA: |
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Database Frequency: | 12 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Cranioectodermal dysplasia 3 | (OMIM:614099) |
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation | (Orphanet:1970) |
HAJDU-CHENEY SYNDROME | (OMIM:102500) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Metaphyseal chondrodysplasia, Kaitila type | (Orphanet:166038) |
Odontomicronychial dysplasia | (Orphanet:1811) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Wrinkly skin syndrome | (Orphanet:2834) |