Thin nail
Symptom Information:
Symptom ID: | HPO:0001816 | ||||||||||||
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) Thin nail(HPO:0001816) MedDRA: |
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Database Frequency: | 11 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant nail dysplasia | (Orphanet:79153) |
Costello syndrome | (Orphanet:3071) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 | (OMIM:242100) |
Odontomicronychial dysplasia | (Orphanet:1811) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
Self-healing collodion baby | (Orphanet:281122) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE I | (OMIM:190350) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |
Weaver syndrome | (Orphanet:3447) |