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239079007: Inherited cutaneous hyperpigmentation (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
358290010 Inherited cutaneous hyperpigmentation en Synonym Active Entire term case insensitive SNOMED CT core module
628047011 Inherited cutaneous hyperpigmentation (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


12 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Inherited cutaneous hyperpigmentation Is a Genodermatosis true Inferred relationship Existential restriction modifier
Inherited cutaneous hyperpigmentation Is a Hyperpigmentation of skin true Inferred relationship Existential restriction modifier
Inherited cutaneous hyperpigmentation Occurrence Congenital false Inferred relationship Existential restriction modifier
Inherited cutaneous hyperpigmentation Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Inherited cutaneous hyperpigmentation Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Inherited cutaneous hyperpigmentation Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 2
Inherited cutaneous hyperpigmentation Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Inherited cutaneous hyperpigmentation Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Inherited cutaneous hyperpigmentation Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Inherited cutaneous hyperpigmentation Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Inherited cutaneous hyperpigmentation Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Inherited cutaneous hyperpigmentation Is a Congenital pigmentary skin anomalies true Inferred relationship Existential restriction modifier
Inherited cutaneous hyperpigmentation Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Inherited cutaneous hyperpigmentation Associated morphology Hyperpigmentation true Inferred relationship Existential restriction modifier 1
Inherited cutaneous hyperpigmentation Is a Genetic disorder of skin pigmentation true Inferred relationship Existential restriction modifier
Inherited cutaneous hyperpigmentation Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Inherited cutaneous hyperpigmentation Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Normal variation in cutaneous pigmentation Is a False Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Dyschromatosis universalis Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Naegeli-Franceschetti-Jadassohn syndrome Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Symmetrical dyschromatosis of extremities Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Zosteriform reticulate hyperpigmentation Is a False Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Dermatopathia pigmentosa reticularis Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Acromelanosis Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Is a False Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Terminal osseous dysplasia and pigmentary defect syndrome Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Thumb deformity, alopecia, pigmentation anomaly syndrome Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Osteopathia striata, pigmentary dermopathy, white forelock syndrome Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Hereditary benign acanthosis nigricans Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Hereditary benign acanthosis nigricans with insulin resistance Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier
Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome Is a True Inherited cutaneous hyperpigmentation Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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