Nail dysplasia
Symptom Information:
Symptom ID: | HPO:0002164 | |||||||||
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 dysplasia(HPO:0002164) MedDRA: |
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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) |