Dry skin

Symptom Information:

Symptom ID: HPO:0000958
Synonyms:
Xerosis [HPO:0000958]
Skin dryness [Orphanet:23170]
Dry skin (finding) [Orphanet:23170]
Dry skin [Orphanet:23170]
Dry skin [OMIM:Dry skin]
Xerosis [OMIM:Xerosis]
Dry/squaly skin/exfoliation [Orphanet:23170]
Xerosis [MedDRA:10048222]
Dry skin [MedDRA:10013786]
Drying [MedDRA:10013786]
Hot dry skin [MedDRA:10013786]
Rough facial skin [MedDRA:10013786]
Skin dry [MedDRA:10013786]
Skin rough [MedDRA:10013786]
Skin roughness [MedDRA:10013786]
Dry scalp [MedDRA:10013786]
Skin xerosis [MedDRA:10013786]
Dry skin aggravated [MedDRA:10013786]
Defatted skin [MedDRA:10013786]
Dry [OMIM:Dry]
Dry scalp [OMIM:Dry scalp]
Rough skin [OMIM:Rough skin]
Xerosis (buttocks, extensor surfaces of extremities) [OMIM:Xerosis (buttocks, extensor surfaces of extremities)]
Skin exfoliation [MedDRA:10040844]
Scaly skin [Orphanet:23170]
Scaly skin (finding) [Orphanet:23170]
Desquamation, function (observable entity) [Orphanet:23170]
Peeling of skin (finding) [Orphanet:23170]
Peeling of skin [Orphanet:23170]
Scaly skin [OMIM:Scaly skin]
Quality:
Cross references:
Orphanet:23170 "Dry/squaly skin/exfoliation" [Orphanet:23170]
OMIM: "Dry skin" [OMIM:Dry skin]
OMIM: "Xerosis" [OMIM:Xerosis]
OMIM: "Dry" [OMIM:Dry]
OMIM: "Dry scalp" [OMIM:Dry scalp]
OMIM: "Rough skin" [OMIM:Rough skin]
OMIM: "Xerosis (buttocks, extensor surfaces of extremities)" [OMIM:Xerosis (buttocks, extensor surfaces of extremities)]
OMIM: "Scaly skin" [OMIM:Scaly skin]
UMLS:C0151908 "Dry skin" [Orphanet:23170]
UMLS:C0237849 "Peeling of skin" [Orphanet:23170]
UMLS:C0423773 "Scaly skin" [Orphanet:23170]
Is a (Direct Parents):
Orphanet Abnormality of the skin
MedDRA General signs and symptoms NEC
MedDRA Dermal and epidermal conditions NEC
HPO         Abnormality of skin morphology
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)
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)