Irregular hyperpigmentation

Symptom Information:

Symptom ID: HPO:0007400
Irregular skin hyperpigmentation [Orphanet:23540]
Irregular hyperpigmentation [OMIM:Irregular hyperpigmentation]
Irregular/in bands/reticular skin hyperpigmentation [Orphanet:23540]
Band skin hyperpigmentation [Orphanet:23540]
Cross references:
Orphanet:23540 "Irregular/in bands/reticular skin hyperpigmentation" [Orphanet:23540]
OMIM: "Irregular hyperpigmentation" [OMIM:Irregular hyperpigmentation]
Is a (Direct Parents):
HPO         Hyperpigmentation of the skin
Orphanet Abnormality of skin pigmentation
Is a (Whole tree): HPO:
    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)
Database Frequency: 72 / 7739

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)
S├ęzary 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)