Hypopigmented skin patches
Symptom Information:
Symptom ID: | HPO:0001053 | ||||||
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) 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: |
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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) |