Dry skin
Symptom Information:
Symptom ID: | HPO:0000958 | ||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||
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 the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Dry skin(HPO:0000958) MedDRA: General disorders and administration site conditions(MedDRA:10018065) General system disorders NEC(MedDRA:10018073) General signs and symptoms NEC(MedDRA:10018072) Dry skin(HPO:0000958) Skin and subcutaneous tissue disorders(MedDRA:10040785) Epidermal and dermal conditions(MedDRA:10014982) Dermal and epidermal conditions NEC(MedDRA:10012424) Dry skin(HPO:0000958) |
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Database Frequency: | 152 / 7739 | ||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
19q13.11 microdeletion syndrome | (Orphanet:217346) |
ADULT syndrome | (Orphanet:978) |
ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS | (OMIM:206600) |
AREDYLD syndrome | (Orphanet:1133) |
Ablepharon macrostomia syndrome | (Orphanet:920) |
Acquired ichthyosis | (Orphanet:454) |
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
Acroosteolysis, dominant type | (Orphanet:955) |
Adiposis dolorosa | (Orphanet:36397) |
Albright hereditary osteodystrophy | (Orphanet:665) |
Alpha-N-acetylgalactosaminidase deficiency type 2 | (Orphanet:79280) |
Alport syndrome | (Orphanet:63) |
Alström syndrome | (Orphanet:64) |
Amelo-onycho-hypohidrotic syndrome | (Orphanet:1028) |
Anonychia with flexural pigmentation | (Orphanet:69125) |
Antisynthetase syndrome | (Orphanet:81) |
Arthrogryposis - hyperkeratosis, lethal form | (Orphanet:1485) |
Ataxia - photosensitivity - short stature | (Orphanet:1184) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
Autosomal recessive palmoplantar keratoderma and congenital alopecia | (Orphanet:1366) |
BRESEK syndrome | (Orphanet:85284) |
Barber-Say syndrome | (Orphanet:1231) |
Biotinidase deficiency | (Orphanet:79241) |
Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
Blau syndrome | (Orphanet:90340) |
Bullous lichen planus | (Orphanet:33408) |
CHILD syndrome | (Orphanet:139) |
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME B | (OMIM:133540) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME | (OMIM:218650) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cataract - deafness - hypogonadism | (Orphanet:1383) |
Central congenital hypothyroidism | (Orphanet:226298) |
Classical mycosis fungoides | (Orphanet:2584) |
Classical phenylketonuria | (Orphanet:79254) |
Cockayne syndrome | (Orphanet:191) |
Congenital hypothyroidism | (Orphanet:442) |
Congenital ichthyosis - intellectual deficit - spastic quadriplegia | (Orphanet:352333) |
Congenital ichthyosis - microcephalus - tetraplegia | (Orphanet:2271) |
Congenital lethal erythroderma | (Orphanet:1954) |
Cranioectodermal dysplasia 3 | (OMIM:614099) |
Cutaneous lupus erythematosus | (Orphanet:535) |
DERMATITIS, ATOPIC | (OMIM:603165) |
DK1-CDG | (Orphanet:91131) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 | (OMIM:613990) |
Dermatomyositis | (Orphanet:221) |
Dermo-odonto dysplasia | (Orphanet:1660) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
Distal trisomy 6p | (Orphanet:1745) |
Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
Dubowitz syndrome | (Orphanet:235) |
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALDOMINANT | (OMIM:614940) |
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE | (OMIM:614941) |
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY | (OMIM:600906) |
EEC syndrome | (Orphanet:1896) |
EPIDERMOLYTIC HYPERKERATOSIS | (OMIM:113800) |
Ectodermal dysplasia - intellectual deficit - central nervous system malformation | (Orphanet:1812) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria | (Orphanet:1035) |
Epidermolysis bullosa simplex due to plakophilin deficiency | (Orphanet:158668) |
Erythrokeratodermia - ataxia | (Orphanet:1955) |
Erythrokeratodermia variabilis | (Orphanet:317) |
Familial melanoma | (Orphanet:618) |
Familial thyroid dyshormonogenesis | (Orphanet:95716) |
Fucosidosis | (Orphanet:349) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Grix-Blankenship-Peterson syndrome | (Orphanet:2099) |
Grubben-de Cock-Borghgraef syndrome | (Orphanet:2101) |
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609943) |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6 | (OMIM:614450) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Hurler syndrome | (Orphanet:93473) |
Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2 | (OMIM:300640) |
Ichthyosis - hypotrichosis - sclerosing cholangitis | (Orphanet:59303) |
Ichthyosis - oral and digital anomalies | (Orphanet:2272) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Intellectual deficit, X-linked - seizures - psoriasis | (Orphanet:3052) |
Intellectual deficit, X-linked, Nascimento type | (Orphanet:163956) |
Isolated thyrotropin-releasing hormone deficiency | (Orphanet:238670) |
Jung-Wolff-Back-Stahl syndrome | (Orphanet:2321) |
Juvenile dermatomyositis | (Orphanet:93672) |
Kawasaki disease | (Orphanet:2331) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Keratosis pilaris atrophicans | (Orphanet:498) |
Kindler syndrome | (Orphanet:2908) |
Koolen-De Vries syndrome | (Orphanet:96169) |
LEOPARD SYNDROME 2 | (OMIM:611554) |
Lamellar ichthyosis | (Orphanet:313) |
Leprechaunism | (Orphanet:508) |
Limited cutaneous systemic sclerosis | (Orphanet:220402) |
Localized scleroderma | (Orphanet:90289) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I | (OMIM:210710) |
MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUALAPPEARANCE | (OMIM:612947) |
MPDU1-CDG | (Orphanet:79323) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
Menkes disease | (Orphanet:565) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C | (OMIM:613216) |
Netherton syndrome | (Orphanet:634) |
Neutral lipid storage disease | (Orphanet:165) |
Oculotrichodysplasia | (Orphanet:2718) |
Odonto-onycho-dermal dysplasia | (Orphanet:2721) |
Odontotrichomelic syndrome | (Orphanet:2723) |
Omenn syndrome | (Orphanet:39041) |
Oral erosive lichen | (Orphanet:31142) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Palmoplantar keratoderma-sclerodactyly syndrome | (Orphanet:384) |
Peeling skin syndrome | (Orphanet:817) |
Pellagra-like skin rash-neurological manifestations | (Orphanet:2837) |
Pemphigus erythematosus | (Orphanet:79480) |
Phenylketonuria | (Orphanet:716) |
Primary cutaneous lymphoma | (Orphanet:542) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Prolidase deficiency | (Orphanet:742) |
RIDDLE SYNDROME | (OMIM:611943) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Recessive X-linked ichthyosis | (Orphanet:461) |
Refsum disease | (Orphanet:773) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |
Rhizomelic chondrodysplasia punctata | (Orphanet:177) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Scleroderma | (Orphanet:801) |
Septo-optic dysplasia | (Orphanet:3157) |
Sjögren-Larsson syndrome | (Orphanet:816) |
Stoll-Alembik-Finck syndrome | (Orphanet:3200) |
Superficial pemphigus | (Orphanet:46485) |
Syndromic X-linked ichthyosis | (Orphanet:281090) |
Sézary syndrome | (Orphanet:3162) |
THYROID DYSHORMONOGENESIS 1 | (OMIM:274400) |
Tangier disease | (Orphanet:31150) |
Thyroid ectopia | (Orphanet:95712) |
Thyroid hemiagenesis | (Orphanet:95719) |
Transgrediens et progrediens palmoplantar keratoderma | (Orphanet:495) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
Trichodysplasia - xeroderma | (Orphanet:3361) |
UV-SENSITIVE SYNDROME 1 | (OMIM:600630) |
UV-SENSITIVE SYNDROME 3 | (OMIM:614640) |
UV-sensitive syndrome | (Orphanet:178338) |
Wrinkly skin syndrome | (Orphanet:2834) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |
XFE PROGEROID SYNDROME | (OMIM:610965) |
Xeroderma pigmentosum | (Orphanet:910) |
Xeroderma pigmentosum variant | (Orphanet:90342) |
Xeroderma pigmentosum/Cockayne syndrome complex | (Orphanet:220295) |
Yunis-Varon syndrome | (Orphanet:3472) |