Hyperpigmentation of the skin
Symptom Information:
Symptom ID: | HPO:0000953 | ||||||||||||||||
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 the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Abnormality of skin pigmentation(HPO:0001000) Hyperpigmentation of the skin(HPO:0000953) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Pigmentation disorders(MedDRA:10035023) Hyperpigmentation disorders(MedDRA:10020713) Hyperpigmentation of the skin(HPO:0000953) |
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Database Frequency: | 75 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
46,XY disorder of sex development - adrenal insufficiency due to CYP11A1 deficiency | (Orphanet:168558) |
ACTH-dependent Cushing syndrome | (Orphanet:99892) |
ADRENAL HYPOPLASIA, CONGENITAL | (OMIM:300200) |
ADRENOCORTICAL UNRESPONSIVENESS TO ACTH WITH POSTRECEPTOR DEFECT | (OMIM:202355) |
ANE syndrome | (Orphanet:157954) |
APC-related attenuated familial adenomatous polyposis | (Orphanet:247806) |
Acanthosis nigricans | (Orphanet:924) |
Acromegaly | (Orphanet:963) |
Addison disease | (Orphanet:85138) |
Adrenomyodystrophy | (Orphanet:977) |
Alström syndrome | (Orphanet:64) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Attenuated familial adenomatous polyposis | (Orphanet:220460) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Becker nevus syndrome | (Orphanet:64755) |
Bullous dystrophy, macular type | (Orphanet:1867) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Castleman disease | (Orphanet:160) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Cockayne syndrome | (Orphanet:191) |
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency | (Orphanet:90795) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Costello syndrome | (Orphanet:3071) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome due to ectopic ACTH secretion | (Orphanet:99889) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 | (OMIM:224230) |
EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATIONAND MICROCEPHALY | (OMIM:133750) |
Familial adenomatous polyposis | (Orphanet:733) |
Familial glucocorticoid deficiency | (Orphanet:361) |
Felty syndrome | (Orphanet:47612) |
Foveal hypoplasia - presenile cataract | (Orphanet:2253) |
GLUCOCORTICOID DEFICIENCY 2 | (OMIM:607398) |
GLUCOCORTICOID DEFICIENCY 3 | (OMIM:609197) |
Gardner syndrome | (Orphanet:79665) |
Gastrointestinal stromal tumor | (Orphanet:44890) |
Gaucher disease type 1 | (Orphanet:77259) |
HYPERPIGMENTATION OF FULDAUER AND KUIJPERS | (OMIM:145200) |
Heart defect - round face - congenital developmental delay | (Orphanet:1355) |
Hemochromatosis type 2 | (Orphanet:79230) |
Hemochromatosis type 3 | (Orphanet:225123) |
Hemochromatosis type 4 | (Orphanet:139491) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hemochromatosis, type 2B | (OMIM:613313) |
Hereditary coproporphyria | (Orphanet:79273) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
McCune-Albright syndrome | (Orphanet:562) |
NASAL HYPERPIGMENTATION, FAMILIAL TRANSVERSE | (OMIM:161530) |
NOONAN SYNDROME 7 | (OMIM:613706) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Neurocutaneous melanocytosis | (Orphanet:2481) |
Neuroectodermal melanolysosomal disease | (Orphanet:33445) |
Neurofibromatosis type 1 | (Orphanet:636) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
Parana hard-skin syndrome | (Orphanet:2812) |
Phakomatosis pigmentovascularis | (Orphanet:2875) |
Porphyria cutanea tarda | (Orphanet:101330) |
Porphyria variegata | (Orphanet:79473) |
Proteus syndrome | (Orphanet:744) |
Pseudoleprechaunism syndrome, Patterson type | (Orphanet:2976) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Sjögren-Larsson syndrome | (Orphanet:816) |
Sparse hair - short stature - skin anomalies | (Orphanet:79132) |
Toriello-Lacassie-Droste syndrome | (Orphanet:3339) |
Triple A syndrome | (Orphanet:869) |
Turcot syndrome with polyposis | (Orphanet:99818) |
Whipple disease | (Orphanet:3452) |
X-linked cerebral adrenoleukodystrophy | (Orphanet:139396) |
Xeroderma pigmentosum | (Orphanet:910) |
Zellweger-like syndrome without peroxisomal anomalies | (Orphanet:50812) |