Thin nail

Symptom Information:

Symptom ID: HPO:0001816
Synonyms:
Thin nails [HPO:0001816]
Thin nail of foot [Orphanet:25400]
Thin nail of hand [Orphanet:25150]
Thin nails [OMIM:Thin nails]
Thin/hypoplastic toenails [Orphanet:25400]
Thin/hypoplastic/hyperconvex fingernails [Orphanet:25150]
Thin nails (rare) [OMIM:Thin nails (rare)]
Quality:
Cross references:
HPO:0001814 "Thin, deep-set nails" [Orphanet:25400]
Orphanet:25400 "Thin/hypoplastic toenails" [Orphanet:25400]
Orphanet:25150 "Thin/hypoplastic/hyperconvex fingernails" [Orphanet:25150]
OMIM: "Thin nails" [OMIM:Thin nails]
OMIM: "Thin nails (rare)" [OMIM:Thin nails (rare)]
Is a (Direct Parents):
Orphanet Abnormality of the toenails
Orphanet Hyperconvex fingernails
HPO         Abnormality of the nail
Orphanet Abnormality of the fingernails
HPO         Thin toenail
HPO         Thin fingernail
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:
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)