Nail pits

Symptom Information:

Symptom ID: HPO:0001803
Synonyms:
Nail pitting [HPO:0001803]
Pitted nails [HPO:0001803]
Pitting of nails [HPO:0001803]
Pitting of nails (disorder) [Orphanet:25750]
Pitting of nails [Orphanet:25750]
Nail pits [OMIM:Nail pits]
Nail pitting [OMIM:Nail pitting]
Pitted nails [OMIM:Pitted nails]
Punctate nails [Orphanet:25750]
Nail pitting [Orphanet:25750]
Nail pitting [MedDRA:10028702]
Pitted nails (rare) [OMIM:Pitted nails (rare)]
Quality:
Cross references:
Orphanet:25750 "Punctate nails" [Orphanet:25750]
OMIM: "Nail pits" [OMIM:Nail pits]
OMIM: "Nail pitting" [OMIM:Nail pitting]
OMIM: "Pitted nails" [OMIM:Pitted nails]
OMIM: "Pitted nails (rare)" [OMIM:Pitted nails (rare)]
UMLS:C0150993 "Pitting of nails" [Orphanet:25750]
Is a (Direct Parents):
HPO         Nail dysplasia
Orphanet Abnormality of the nail
MedDRA Nail and nail bed conditions (excl infections and infestations)
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)
                Nail dysplasia(HPO:0002164)
                   Nail pits(HPO:0001803)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin appendage conditions(MedDRA:10040798)
       Nail and nail bed conditions (excl infections and infestations)(MedDRA:10028685)
          Nail pits(HPO:0001803)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

ADULT syndrome (Orphanet:978)
ALOPECIA AREATA 1 (OMIM:104000)
Alopecia totalis (Orphanet:700)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 (OMIM:127550)
Dyskeratosis congenita (Orphanet:1775)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
HYPOTRICHOSIS 8 (OMIM:278150)
Hypodontia - dysplasia of nails (Orphanet:2228)
Hypotrichosis simplex (Orphanet:55654)
Incontinentia pigmenti (Orphanet:464)
Juvenile idiopathic arthritis (Orphanet:92)
PSORIASIS 1, SUSCEPTIBILITY TO (OMIM:177900)
Pediatric systemic sclerosis (Orphanet:93567)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)
Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy (Orphanet:169095)