Nail dysplasia

Symptom Information:

Symptom ID: HPO:0002164
Synonyms:
Dysplastic nails [HPO:0002164]
Onychodysplasia [HPO:0002164]
Dysplastic nails [OMIM:Dysplastic nails]
Nail dysplasia [OMIM:Nail dysplasia]
Onychodysplasia [OMIM:Onychodysplasia]
Dysplastic nails (1st and 2nd toes) [OMIM:Dysplastic nails (1st and 2nd toes)]
Nail dysplasia (22%) [OMIM:Nail dysplasia (22%)]
Nail dysplasia (35%) [OMIM:Nail dysplasia (35%)]
Onychodysplasia (40%) [OMIM:Onychodysplasia (40%)]
Quality:
Cross references:
OMIM: "Dysplastic nails" [OMIM:Dysplastic nails]
OMIM: "Nail dysplasia" [OMIM:Nail dysplasia]
OMIM: "Onychodysplasia" [OMIM:Onychodysplasia]
OMIM: "Dysplastic nails (1st and 2nd toes)" [OMIM:Dysplastic nails (1st and 2nd toes)]
OMIM: "Nail dysplasia (22%)" [OMIM:Nail dysplasia (22%)]
OMIM: "Nail dysplasia (35%)" [OMIM:Nail dysplasia (35%)]
OMIM: "Onychodysplasia (40%)" [OMIM:Onychodysplasia (40%)]
Is a (Direct Parents):
HPO         Abnormality of the nail
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)
MedDRA:
Database Frequency: 82 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
2q32q33 microdeletion syndrome (Orphanet:251019)
ADULT syndrome (Orphanet:978)
ALG3-CDG (Orphanet:79321)
ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY (OMIM:106990)
Acrofacial dysostosis, Weyers type (Orphanet:952)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal dominant nail dysplasia (Orphanet:79153)
Autosomal dominant palmoplantar keratoderma and congenital alopecia (Orphanet:1010)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive deafness-onychodystrophy syndrome (Orphanet:79500)
Autosomal recessive palmoplantar keratoderma and congenital alopecia (Orphanet:1366)
Bathing suit ichthyosis (Orphanet:100976)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
CHANDS (OMIM:214350)
Coats plus syndrome (Orphanet:313838)
Congenital anonychia (Orphanet:79143)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
Cooks syndrome (Orphanet:1487)
Cronkhite-Canada syndrome (Orphanet:2930)
DPM1-CDG (Orphanet:79322)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 (OMIM:613989)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 (OMIM:613990)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 (OMIM:224230)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2 (OMIM:613987)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3 (OMIM:613988)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Dermo-odonto dysplasia (Orphanet:1660)
Dystrophic epidermolysis bullosa pruriginosa (Orphanet:89843)
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT (OMIM:129490)
ECTODERMAL DYSPLASIA WITH ADRENAL CYST (OMIM:129550)
EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA (OMIM:226500)
EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN ANDDEFORMITY OF NAILS (OMIM:132000)
Ellis Van Creveld syndrome (Orphanet:289)
Epidermolysis bullosa simplex with mottled pigmentation (Orphanet:79397)
Epidermolysis bullosa simplex with muscular dystrophy (Orphanet:257)
Epidermolysis bullosa simplex, Dowling-Meara type (Orphanet:79396)
Focal dermal hypoplasia (Orphanet:2092)
Generalized dominant dystrophic epidermolysis bullosa (Orphanet:231568)
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type (Orphanet:79399)
Generalized pustular psoriasis (Orphanet:247353)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hereditary sensory and autonomic neuropathy type 4 (Orphanet:642)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit, X-linked, Nascimento type (Orphanet:163956)
Junctional epidermolysis bullosa - pyloric atresia (Orphanet:79403)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (OMIM:612843)
KID syndrome (Orphanet:477)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
Leprechaunism (Orphanet:508)
Limb-mammary syndrome (Orphanet:69085)
Localized junctional epidermolysis bullosa, non-Herlitz type (Orphanet:251393)
Mammary-digital-nail syndrome (Orphanet:238744)
Monilethrix (Orphanet:573)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
NEUROPATHY, HEREDITARY SENSORY, TYPE ID (OMIM:613708)
Oculotrichodysplasia (Orphanet:2718)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Odonto-tricho-ungual-digito-palmar syndrome (Orphanet:69082)
Otopalatodigital syndrome type 1 (Orphanet:90650)
PACHYONYCHIA CONGENITA 2 (OMIM:167210)
PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS (OMIM:600399)
POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY,AND PULMONARY FIBROSIS (OMIM:615704)
Pallister-Hall syndrome (Orphanet:672)
Palmoplantar keratoderma-spastic paralysis syndrome (Orphanet:2201)
Rosselli-Gulienetti syndrome (Orphanet:90339)
SABINAS BRITTLE HAIR SYNDROME (OMIM:211390)
SCLEROSTEOSIS 1 (OMIM:269500)
SCLEROSTEOSIS 2 (OMIM:614305)
Scalp-ear-nipple syndrome (Orphanet:2036)
Sclerosteosis (Orphanet:3152)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Skin fragility-woolly hair-palmoplantar keratoderma syndrome (Orphanet:293165)
Tangier disease (Orphanet:31150)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Tricho-odonto-onychial dysplasia (Orphanet:3355)
Zlotogora-Ogur syndrome (Orphanet:3253)