Anonychia

Symptom Information:

Symptom ID: HPO:0001798
Synonyms:
Absent nails [HPO:0001798]
Aplastic nails [HPO:0001798]
ANONYCHIA [HPO:0001798]
Absent nails [OMIM:Absent nails]
Anonychia [OMIM:Anonychia]
Quality:
Cross references:
OMIM: "Absent nails" [OMIM:Absent nails]
OMIM: "Anonychia" [OMIM:Anonychia]
UMLS:C0265998 "ANONYCHIA" [HPO:0001798]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the nails
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)
                   Anonychia(HPO:0001798)
MedDRA:
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

ANONYCHIA-ECTRODACTYLY (OMIM:106900)
ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY (OMIM:106990)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Anonychia congenita totalis (Orphanet:94150)
Anonychia with flexural pigmentation (Orphanet:69125)
Autosomal recessive deafness-onychodystrophy syndrome (Orphanet:79500)
Bartsocas-Papas syndrome (Orphanet:1234)
Brachydactyly type B (Orphanet:93383)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
Congenital anonychia (Orphanet:79143)
Cooks syndrome (Orphanet:1487)
Deafness - onychodystrophy (Orphanet:3231)
Deafness - onychodystrophy, autosomal dominant (Orphanet:79499)
Distal symphalangism (Orphanet:3248)
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME (OMIM:616029)
Fryns syndrome (Orphanet:2059)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Junctional epidermolysis bullosa - pyloric atresia (Orphanet:79403)
Lethal acantholytic epidermolysis bullosa (Orphanet:158687)
Mammary-digital-nail syndrome (Orphanet:238744)
Multiple synostoses syndrome (Orphanet:3237)
Nail-patella syndrome (Orphanet:2614)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Phocomelia, Schinzel type (Orphanet:2879)
SANTOS SYNDROME (OMIM:613005)
SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH (OMIM:606895)
SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL (OMIM:186400)
Tarsal-carpal coalition syndrome (Orphanet:1412)