Nail dystrophy
Symptom Information:
Symptom ID: | HPO:0008404 | ||||||||||||||||||||
Synonyms: |
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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) Nail dystrophy(HPO:0008404) 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 dystrophy(HPO:0008404) |
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Database Frequency: | 89 / 7739 | ||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
ANGIOMA SERPIGINOSUM, X-LINKED | (OMIM:300652) |
ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY | (OMIM:106990) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Autosomal recessive deafness-onychodystrophy syndrome | (Orphanet:79500) |
Autosomal recessive palmoplantar keratoderma and congenital alopecia | (Orphanet:1366) |
BRESEK syndrome | (Orphanet:85284) |
Bathing suit ichthyosis | (Orphanet:100976) |
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION | (OMIM:601088) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Congenital anonychia | (Orphanet:79143) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Cooks syndrome | (Orphanet:1487) |
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis | (Orphanet:352662) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 | (OMIM:127550) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 | (OMIM:613989) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 | (OMIM:224230) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2 | (OMIM:613987) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3 | (OMIM:613988) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 5 | (OMIM:615190) |
Deafness - onychodystrophy | (Orphanet:3231) |
Deafness - onychodystrophy, autosomal dominant | (Orphanet:79499) |
Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
Dermatopathia pigmentosa reticularis | (Orphanet:86920) |
Disseminated superficial actinic porokeratosis | (Orphanet:79152) |
Distal limb deficiencies - micrognathia syndrome | (Orphanet:1307) |
Dyschromatosis universalis hereditaria 1 | (OMIM:127500) |
Dyschromatosis universalis hereditaria 2 | (OMIM:612715) |
Dyschromatosis universalis hereditaris 3 | (OMIM:615402) |
Dyskeratosis congenita | (Orphanet:1775) |
Dystrophic epidermolysis bullosa pruriginosa | (Orphanet:89843) |
ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE | (OMIM:602032) |
ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE | (OMIM:614931) |
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME | (OMIM:616029) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA | (OMIM:226500) |
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2 | (OMIM:615425) |
EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN ANDDEFORMITY OF NAILS | (OMIM:132000) |
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 junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:79402) |
Generalized pustular psoriasis | (Orphanet:247353) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
Hereditary sensory and autonomic neuropathy type 4 | (Orphanet:642) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hidrotic ectodermal dysplasia, Christianson-Fourie type | (Orphanet:1808) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
IMMUNODEFICIENCY, COMMON VARIABLE, 10 | (OMIM:615577) |
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 inversa | (Orphanet:79405) |
Junctional epidermolysis bullosa, Herlitz type | (Orphanet:79404) |
Junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:89840) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT | (OMIM:612843) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED | (OMIM:308800) |
KID syndrome | (Orphanet:477) |
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome | (Orphanet:281201) |
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) |
NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6 | (OMIM:107000) |
NEUROPATHY, HEREDITARY SENSORY, TYPE ID | (OMIM:613708) |
Naxos disease | (Orphanet:34217) |
Nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome | (Orphanet:300333) |
Odonto-tricho-ungual-digito-palmar syndrome | (Orphanet:69082) |
Otopalatodigital syndrome type 1 | (Orphanet:90650) |
PACHYONYCHIA CONGENITA 2 | (OMIM:167210) |
PACHYONYCHIA CONGENITA 3 | (OMIM:615726) |
PACHYONYCHIA CONGENITA 4 | (OMIM:615728) |
PSORIASIS 15, PUSTULAR, SUSCEPTIBILITY TO | (OMIM:616106) |
Palmoplantar keratoderma-spastic paralysis syndrome | (Orphanet:2201) |
Pure hair and nail ectodermal dysplasia | (Orphanet:69084) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Retinopathy - anemia- central nervous system anomalies | (Orphanet:3088) |
SABINAS BRITTLE HAIR SYNDROME | (OMIM:211390) |
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET | (OMIM:615934) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Skin fragility-woolly hair-palmoplantar keratoderma syndrome | (Orphanet:293165) |
Tangier disease | (Orphanet:31150) |
Transient bullous dermolysis of the newborn | (Orphanet:79411) |
Tricho-odonto-onychial dysplasia | (Orphanet:3355) |