Irregular hyperpigmentation
Symptom Information:
Symptom ID: | HPO:0007400 | ||||
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) Hyperpigmentation of the skin(HPO:0000953) Irregular hyperpigmentation(HPO:0007400) MedDRA: |
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Database Frequency: | 72 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Ackerman syndrome | (Orphanet:2561) |
Acrogeria | (Orphanet:2500) |
Acromelanosis | (Orphanet:39) |
Albinism-deafness syndrome | (Orphanet:998) |
Alkaptonuria | (Orphanet:56) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Bloom syndrome | (Orphanet:125) |
Classical mycosis fungoides | (Orphanet:2584) |
Cutaneous lupus erythematosus | (Orphanet:535) |
Deaf blind hypopigmentation syndrome, Yemenite type | (Orphanet:3214) |
Dyschromatosis symmetrica hereditaria | (Orphanet:41) |
Dyschromatosis universalis | (Orphanet:241) |
Dyskeratosis congenita | (Orphanet:1775) |
Ectodermal dysplasia, Berlin type | (Orphanet:1816) |
Ectodermal dysplasia, tricho-odonto-onychial type | (Orphanet:1818) |
Ermine phenotype | (Orphanet:999) |
Erythrokeratodermia variabilis | (Orphanet:317) |
Extrasystoles - short stature - hyperpigmentation - microcephaly | (Orphanet:1964) |
Familial adenomatous polyposis | (Orphanet:733) |
Familial multiple nevi flammei | (Orphanet:624) |
Fanconi anemia | (Orphanet:84) |
Felty syndrome | (Orphanet:47612) |
Focal facial dermal dysplasia | (Orphanet:79133) |
Gastrointestinal stromal tumor | (Orphanet:44890) |
Hartnup syndrome | (Orphanet:2116) |
Hennekam-Beemer syndrome | (Orphanet:2135) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hyperkeratosis-hyperpigmentation syndrome | (Orphanet:1336) |
Hypo- and hypermelanotic cutaneous macules - retarded growth - intellectual deficiency | (Orphanet:2435) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
Incontinentia pigmenti | (Orphanet:464) |
Infantile myofibromatosis | (Orphanet:2591) |
Intellectual deficit - hypotonia - skin hyperpigmentation | (Orphanet:3050) |
Junctional epidermolysis bullosa | (Orphanet:305) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
Mosaic trisomy 8 | (Orphanet:96061) |
Multiple benign circumferential skin creases on limbs | (Orphanet:2505) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Naegeli-Franceschetti-Jadassohn syndrome | (Orphanet:69087) |
Netherton syndrome | (Orphanet:634) |
PARC syndrome | (Orphanet:2825) |
POEMS syndrome | (Orphanet:2905) |
Piebald trait - neurologic defects | (Orphanet:2885) |
Piebaldism | (Orphanet:2884) |
Pilodental dysplasia - refractive errors | (Orphanet:2892) |
Pityriasis rubra pilaris | (Orphanet:2897) |
Porphyria cutanea tarda | (Orphanet:101330) |
Porphyria due to ALA dehydratase deficiency | (Orphanet:100924) |
Primary cutaneous lymphoma | (Orphanet:542) |
Progressive hemifacial atrophy | (Orphanet:1214) |
Proteus syndrome | (Orphanet:744) |
Proteus-like syndrome | (Orphanet:2969) |
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia | (Orphanet:3390) |
Reynolds syndrome | (Orphanet:779) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Rothmund-Thomson syndrome type 1 | (Orphanet:221008) |
Sea-blue histiocytosis | (Orphanet:158029) |
Spastic paraplegia - facial-cutaneous lesions | (Orphanet:2819) |
Spastic paraplegia - neuropathy - poikiloderma | (Orphanet:2821) |
Steatocystoma multiplex - natal teeth | (Orphanet:3184) |
Subcorneal pustular dermatosis | (Orphanet:48377) |
Sézary syndrome | (Orphanet:3162) |
Thumb deformity - alopecia - pigmentation anomaly | (Orphanet:2251) |
Torg-Winchester syndrome | (Orphanet:3460) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
WT limb-blood syndrome | (Orphanet:3466) |
X-linked sideroblastic anemia | (Orphanet:75563) |
Xeroderma pigmentosum | (Orphanet:910) |