Hypopigmented skin patches

Symptom Information:

Symptom ID: HPO:0001053
Synonyms:
Hypopigmented skin patch [Orphanet:23520]
Hypopigmented skin patches [OMIM:Hypopigmented skin patches]
Irregular/patchy skin hypopigmentation [Orphanet:23520]
Quality:
Cross references:
HPO:0005590 "Spotty hypopigmentation" [Orphanet:23520]
Orphanet:23520 "Irregular/patchy skin hypopigmentation" [Orphanet:23520]
OMIM: "Hypopigmented skin patches" [OMIM:Hypopigmented skin patches]
Is a (Direct Parents):
Orphanet Abnormality of skin pigmentation
HPO         Localized skin lesion
HPO         Hypopigmentation of the skin
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)
                   Abnormality of skin pigmentation(HPO:0001000)
                      Hypopigmentation of the skin(HPO:0001010)
                         Hypopigmented skin patches(HPO:0001053)
             Localized skin lesion(HPO:0011355)
                Hypopigmented skin patches(HPO:0001053)
MedDRA:
Database Frequency: 80 / 7739
Resource:

All diseases associated with this symptom:

Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
Albinism-deafness syndrome (Orphanet:998)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
Bloom syndrome (Orphanet:125)
Brachytelephalangy - dysmorphism - Kallmann syndrome (Orphanet:1295)
Branchiogenic deafness syndrome (Orphanet:50815)
Classical mycosis fungoides (Orphanet:2584)
Cowden syndrome (Orphanet:201)
Cronkhite-Canada syndrome (Orphanet:2930)
Crouzon disease (Orphanet:207)
Curry-Jones syndrome (Orphanet:1553)
Deaf blind hypopigmentation syndrome, Yemenite type (Orphanet:3214)
Deafness - vitiligo - achalasia (Orphanet:3239)
Dyschromatosis symmetrica hereditaria (Orphanet:41)
Dyschromatosis universalis (Orphanet:241)
Dyskeratosis congenita (Orphanet:1775)
Dystrophic epidermolysis bullosa (Orphanet:303)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Epidermodysplasia verruciformis (Orphanet:302)
Epidermolysis bullosa simplex with mottled pigmentation (Orphanet:79397)
Epiphyseal dysplasia - hearing loss - dysmorphism (Orphanet:1825)
Ermine phenotype (Orphanet:999)
Facial ectodermal dysplasia (Orphanet:1807)
Familial progressive hyperpigmentation (Orphanet:79146)
Fanconi anemia (Orphanet:84)
GAPO syndrome (Orphanet:2067)
Gemignani syndrome (Orphanet:2074)
Generalized dominant dystrophic epidermolysis bullosa (Orphanet:231568)
Griscelli disease (Orphanet:381)
Griscelli disease type 2 (Orphanet:79477)
Harrod syndrome (Orphanet:2115)
Hartnup syndrome (Orphanet:2116)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hypo- and hypermelanotic cutaneous macules - retarded growth - intellectual deficiency (Orphanet:2435)
Incontinentia pigmenti (Orphanet:464)
Ito hypomelanosis (Orphanet:435)
Large congenital melanocytic nevus (Orphanet:626)
Lichen planopilaris (Orphanet:525)
Limited cutaneous systemic sclerosis (Orphanet:220402)
Localized scleroderma (Orphanet:90289)
MELAS (Orphanet:550)
Mandibuloacral dysplasia (Orphanet:2457)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Mosaic trisomy 8 (Orphanet:96061)
Neurofibromatosis type 1 (Orphanet:636)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
Oculo-reno-cerebellar syndrome (Orphanet:2715)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Papillon-Lefèvre syndrome (Orphanet:678)
Phakomatosis pigmentovascularis (Orphanet:2875)
Piebald trait - neurologic defects (Orphanet:2885)
Piebaldism (Orphanet:2884)
Pitt-Hopkins syndrome (Orphanet:2896)
Porphyria cutanea tarda (Orphanet:101330)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Primary cutaneous lymphoma (Orphanet:542)
Rothmund-Thomson syndrome (Orphanet:2909)
Rothmund-Thomson syndrome type 1 (Orphanet:221008)
Ruvalcaba syndrome (Orphanet:3121)
Scleroderma (Orphanet:801)
Spastic paraplegia - facial-cutaneous lesions (Orphanet:2819)
Sternal malformation - vascular dysplasia (Orphanet:3195)
Thumb deformity - alopecia - pigmentation anomaly (Orphanet:2251)
Transient bullous dermolysis of the newborn (Orphanet:79411)
Tuberous sclerosis (Orphanet:805)
Tumoral calcinosis (Orphanet:53715)
Vogt-Koyanagi-Harada disease (Orphanet:3437)
WAARDENBURG SYNDROME, TYPE 2E (OMIM:611584)
WAARDENBURG SYNDROME, TYPE 4A (OMIM:277580)
WAARDENBURG SYNDROME, TYPE 4B (OMIM:613265)
WAARDENBURG SYNDROME, TYPE 4C (OMIM:613266)
Waardenburg syndrome (Orphanet:3440)
Waardenburg syndrome type 1 (Orphanet:894)
Waardenburg syndrome type 2 (Orphanet:895)
Waardenburg syndrome type 3 (Orphanet:896)
Waardenburg-Shah syndrome (Orphanet:897)
X-linked agammaglobulinemia (Orphanet:47)
Xeroderma pigmentosum (Orphanet:910)