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49765009: Hyperpigmentation of skin (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
82896013 Hyperpigmentation of skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
495498012 Hyperpigmentation disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
495499016 Hyperpigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
787479017 Hyperpigmentation of skin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1856721000195117 iperpigmentazione cutanea it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
123701000077114 hyperpigmentation de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
577541000274115 Hyperpigmentierung der Haut de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


153 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperpigmentation of skin Is a Skin lesion false Inferred relationship Some
Hyperpigmentation of skin Is a Acquired disorder of skin colour false Inferred relationship Some
Hyperpigmentation of skin Finding site Skin structure false Inferred relationship Some 1
Hyperpigmentation of skin Finding site Structure of skin region false Inferred relationship Some 1
Hyperpigmentation of skin Associated morphology Hyperpigmentation false Inferred relationship Some 1
Hyperpigmentation of skin Is a Site-specific disorder of skin false Inferred relationship Some
Hyperpigmentation of skin Finding site Skin structure false Inferred relationship Some 1
Hyperpigmentation of skin Is a Degenerative disorder false Inferred relationship Some
Hyperpigmentation of skin Finding site Skin structure true Inferred relationship Some 1
Hyperpigmentation of skin Associated morphology Hyperpigmentation true Inferred relationship Some 1
Hyperpigmentation of skin Is a Disorder of skin pigmentation (disorder) true Inferred relationship Some
Hyperpigmentation of skin Is a Skin deposits true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Acquired hypermelanotic disorder Is a True Hyperpigmentation of skin Inferred relationship Some
Inherited cutaneous hyperpigmentation Is a True Hyperpigmentation of skin Inferred relationship Some
Mercury pigmentation of skin Is a False Hyperpigmentation of skin Inferred relationship Some
Acquired lentiginosis Is a False Hyperpigmentation of skin Inferred relationship Some
Traumatic hemorrhage into heel that persists as black dots. Is a False Hyperpigmentation of skin Inferred relationship Some
Carotene pigmentation of skin Is a False Hyperpigmentation of skin Inferred relationship Some
Pigmented hairy epidermal nevus Is a True Hyperpigmentation of skin Inferred relationship Some
Chrysoderma Is a False Hyperpigmentation of skin Inferred relationship Some
Inflammatory hyperkeratotic dermatosis Is a False Hyperpigmentation of skin Inferred relationship Some
Inflammatory hyperkeratotic dermatosis, chronic Is a False Hyperpigmentation of skin Inferred relationship Some
Inflammatory hyperkeratotic dermatosis, isomorphous Is a False Hyperpigmentation of skin Inferred relationship Some
Inflammatory hyperkeratotic dermatosis, intertriginous Is a False Hyperpigmentation of skin Inferred relationship Some
Inflammatory hyperkeratotic dermatosis, annular Is a False Hyperpigmentation of skin Inferred relationship Some
Inflammatory hyperkeratotic dermatosis, plaque Is a False Hyperpigmentation of skin Inferred relationship Some
Inflammatory hyperkeratotic dermatosis, rupial Is a False Hyperpigmentation of skin Inferred relationship Some
Inflammatory hyperkeratotic dermatosis, guttate Is a False Hyperpigmentation of skin Inferred relationship Some
Inflammatory hyperkeratotic dermatosis, generalized exfoliative Is a False Hyperpigmentation of skin Inferred relationship Some
Lentigo simplex (disorder) Is a False Hyperpigmentation of skin Inferred relationship Some
Arsenic-induced skin pigmentation (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Hereditary hypermelanosis (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Zosteriform reticulate hyperpigmentation Is a True Hyperpigmentation of skin Inferred relationship Some
Lichen planus (LP) pigmentosus is a rare variant of cutaneous lichen planus characterized by the presence of hyperpigmented lichenoid lesions in sun-exposed or flexural areas of the body. Is a True Hyperpigmentation of skin Inferred relationship Some
A rare genetic neurological disease characterized by silvery hair, profound dysfunction of central nervous system, abnormal melanocytes and melanosomes and abnormal inclusion bodies in fibroblast and other cells. Is a True Hyperpigmentation of skin Inferred relationship Some
A rare, syndromic, hyperpigmentation of the skin characterized by multiple lentigines and café-au-lait spots associated with hiatal hernia and peptic ulcer, hypertelorism and myopia. There have been no further descriptions in the literature since 1982. Is a True Hyperpigmentation of skin Inferred relationship Some
Riehl's melanosis Is a True Hyperpigmentation of skin Inferred relationship Some
Benign acanthosis nigricans Is a True Hyperpigmentation of skin Inferred relationship Some
Solar lentiginosis Is a True Hyperpigmentation of skin Inferred relationship Some
Cantu's syndrome Is a True Hyperpigmentation of skin Inferred relationship Some
Reticulate acropigmentation of Kitamura Is a True Hyperpigmentation of skin Inferred relationship Some
Hypotrichosis with keratosis pilaris and lentiginosis Is a True Hyperpigmentation of skin Inferred relationship Some
Post-inflammatory hyperpigmentation Is a True Hyperpigmentation of skin Inferred relationship Some
Drug-induced hypermelanosis Is a True Hyperpigmentation of skin Inferred relationship Some
Eruptive lentiginosis Is a True Hyperpigmentation of skin Inferred relationship Some
Genital lentiginosis Is a True Hyperpigmentation of skin Inferred relationship Some
Diabetic dermopathy Is a True Hyperpigmentation of skin Inferred relationship Some
Circumscribed hypermelanosis (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Lentiginosis due to PUVA Is a True Hyperpigmentation of skin Inferred relationship Some
Nevoid lentiginosis (disorder) Is a False Hyperpigmentation of skin Inferred relationship Some
Hyperchromic lesions of pinta Is a True Hyperpigmentation of skin Inferred relationship Some
Solar lentigo Is a True Hyperpigmentation of skin Inferred relationship Some
Vulval melanotic macule (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Melanotic macule of penis (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Acquired acanthosis nigricans Is a True Hyperpigmentation of skin Inferred relationship Some
A rare endocrine disease characterized by lentigines with a specific peri-orifical distribution, blue nevus, myxomas, various endocrine tumors including primary pigmented nodular adrenocortical disease (PPNAD), acromegaly, thyroid tumors, and a wide range of other tumors. Is a True Hyperpigmentation of skin Inferred relationship Some
Pseudoleprechaunism syndrome, Patterson type is a rare, genetic, adrenal disorder characterized by congenital bronzed hyperpigmentation, cutis laxa of the hands and feet, body disproportion (comprising large hands, feet, nose and ears), hirsutism and severe intellectual disability. Patients additionally present hyperadrenocorticism, cushingoid features, premature adrenarche and diabetes mellitus, as well as skeletal deformities (not present at birth and which progress with age). There have been no further descriptions in the literature since 1981. Is a True Hyperpigmentation of skin Inferred relationship Some
Carney complex-trismus-pseudocamptodactyly syndrome is a rare genetic heart-hand syndrome characterized by typical manifestations of the Carney complex (spotty pigmentation of the skin, familial cardiac and cutaneous myxomas and endocrinopathy) associated with trismus and distal arthrogryposis (presenting as involuntary contraction of distal and proximal interphalangeal joints of hands evident only on dorsiflexion of wrist and similar lower-limb contractures producing foot deformities). Is a True Hyperpigmentation of skin Inferred relationship Some
Erythromelanosis follicularis of face AND/OR neck Is a True Hyperpigmentation of skin Inferred relationship Some
Zosteriform lentiginosis (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Hyperpigmentation of eyelid Is a True Hyperpigmentation of skin Inferred relationship Some
Progressive cribriform and zosteriform hyperpigmentation (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Legius syndrome Is a True Hyperpigmentation of skin Inferred relationship Some
X-linked reticulate pigmentary disorder is an extremely rare skin disease described in only four families to date and characterized in males by diffuse reticulate brown hyperpigmented skin lesions developing in early childhood and a variety of systemic manifestations (recurrent pneumonia, corneal opacification, gastrointestinal inflammation, urethral stricture, failure to thrive, hypohidrosis, digital clubbing, and unruly hair and flared eyebrows), while in females, there is only cutaneous involvement with the development in early childhood of localized brown hyperpigmented skin lesions following the lines of Blaschko. This disease was first considered as a cutaneous amyloidosis, but amyloid deposits are an inconstant feature. Is a True Hyperpigmentation of skin Inferred relationship Some
A rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability characterized by infantile onset of global developmental delay, severe intellectual disability, growth deficiency, microcephaly, strabismus, blue-gray sclerae, and extensive Mongolian spots. Some patients also present with epilepsy. Brain imaging may demonstrate variable abnormalities including cerebral atrophy, thin corpus callosum, ventriculomegaly, or arachnoid cysts. Is a True Hyperpigmentation of skin Inferred relationship Some
Neurofibromatosis type 6 (NF6), also referred as café-au-lait spots syndrome, is a cutaneous disorder characterized by the presence of several café-au-lait (CAL) macules without any other manifestations of neurofibromatosis or any other systemic disorder. Is a True Hyperpigmentation of skin Inferred relationship Some
Skin graft hyperpigmentation (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Hyperpigmentation of right eyelid and periocular area (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Hyperpigmentation of left eyelid and periocular area (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Hypermelanosis caused by photodynamic agent (disorder) Is a False Hyperpigmentation of skin Inferred relationship Some
A combination of congenital hyperpigmented and hypopigmented skin lesions coexisting in the same individual. Is a True Hyperpigmentation of skin Inferred relationship Some
Nevus spilus (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Dermal melanocytic hamartoma (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Linear atrophoderma of Moulin (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
A rare mosaic form of Legius syndrome with findings typical of Legius syndrome, namely multiple cafe-au-lait macules (CALMs) with or without axillary or inguinal freckling. Mosaic form is caused by postzygotic pathogenic variants in SPRED1 gene. In mosaic Legius syndrome the allelic/tissue distribution of the pathogenic SPRED1-variant clearly suggests mosaicism and/or the distribution of CALMs is segmental. The phenotype can be milder than in Legius syndrome. Is a True Hyperpigmentation of skin Inferred relationship Some
Hypermelanosis due to neoplasia (disorder) Is a True Hyperpigmentation of skin Inferred relationship Some
Acanthosis palmaris Is a True Hyperpigmentation of skin Inferred relationship Some

This concept is not in any reference sets

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