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205564003: Congenital pigmentary skin anomalies (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
315243010 Congenital pigmentary skin anomalies en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
590950015 Congenital pigmentary skin anomalies (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2475672012 Congenital pigmentary anomaly of skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
111761000172114 anomalies congénitales de pigmentation de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
113081000172115 congenitale pigmentafwijkingen van huid nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


60 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital pigmentary skin anomalies Is a Congenital anomaly of tongue false Inferred relationship Some
Congenital pigmentary skin anomalies Is a Congenital anomaly of integument false Inferred relationship Some
Congenital pigmentary skin anomalies Is a Congenital heart disease false Inferred relationship Some
Congenital pigmentary skin anomalies Finding site Structure of skin region false Inferred relationship Some 1
Congenital pigmentary skin anomalies Associated morphology Congenital malformation false Inferred relationship Some
Congenital pigmentary skin anomalies Finding site Jaw region structure false Inferred relationship Some
Congenital pigmentary skin anomalies Associated morphology Congenital anomaly false Inferred relationship Some 1
Congenital pigmentary skin anomalies Occurrence Congenital false Inferred relationship Some
Congenital pigmentary skin anomalies Finding site Upper gastrointestinal tract structure false Inferred relationship Some
Congenital pigmentary skin anomalies Finding site Heart structure false Inferred relationship Some
Congenital pigmentary skin anomalies Finding site Tongue structure false Inferred relationship Some 1
Congenital pigmentary skin anomalies Associated morphology Congenital anomaly false Inferred relationship Some 1
Congenital pigmentary skin anomalies Finding site Cardiovascular system subdivision false Inferred relationship Some 2
Congenital pigmentary skin anomalies Is a Congenital anomaly of skin true Inferred relationship Some
Congenital pigmentary skin anomalies Is a Site-specific disorder of skin false Inferred relationship Some
Congenital pigmentary skin anomalies Is a Disorder of skin pigmentation (disorder) true Inferred relationship Some
Congenital pigmentary skin anomalies Associated morphology Pigment alteration false Inferred relationship Some 2
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Some 1
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Some 2
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Some 2
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Some 1
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Some 2
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Some 1
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Some 1
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Some 2
Congenital pigmentary skin anomalies Occurrence Congenital false Inferred relationship Some 3
Congenital pigmentary skin anomalies Associated morphology Developmental anomaly false Inferred relationship Some 3
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Some 3
Congenital pigmentary skin anomalies Occurrence Congenital true Inferred relationship Some 1
Congenital pigmentary skin anomalies Associated morphology Pigment alteration true Inferred relationship Some 1
Congenital pigmentary skin anomalies Finding site Skin structure true Inferred relationship Some 1
Congenital pigmentary skin anomalies Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital pigmentary skin anomaly NOS Is a False Congenital pigmentary skin anomalies Inferred relationship Some
Congenital deficiency of pigment of skin Is a True Congenital pigmentary skin anomalies Inferred relationship Some
Terminal osseous dysplasia and pigmentary defect syndrome (disorder) Is a False Congenital pigmentary skin anomalies Inferred relationship Some
Neuroectodermal melanolysosomal disease (disorder) Is a True Congenital pigmentary skin anomalies Inferred relationship Some
Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome Is a True Congenital pigmentary skin anomalies Inferred relationship Some
Carney complex (disorder) Is a True Congenital pigmentary skin anomalies Inferred relationship Some
Familial progressive hyper and hypopigmentation Is a True Congenital pigmentary skin anomalies Inferred relationship Some
Carney complex, trismus, pseudocamptodactyly syndrome Is a True Congenital pigmentary skin anomalies Inferred relationship Some
Hereditary benign acanthosis nigricans Is a False Congenital pigmentary skin anomalies Inferred relationship Some
Hereditary benign acanthosis nigricans with insulin resistance Is a False Congenital pigmentary skin anomalies Inferred relationship Some
Hypotrichosis with keratosis pilaris and lentiginosis Is a False Congenital pigmentary skin anomalies Inferred relationship Some
Peutz-Jeghers syndrome Is a False Congenital pigmentary skin anomalies Inferred relationship Some
Familial generalised lentiginosis Is a True Congenital pigmentary skin anomalies Inferred relationship Some
Centrofacial lentiginosis syndrome Is a False Congenital pigmentary skin anomalies Inferred relationship Some
Inherited cutaneous hyperpigmentation Is a True Congenital pigmentary skin anomalies Inferred relationship Some
Pseudoleprechaunism syndrome Patterson type (disorder) Is a True Congenital pigmentary skin anomalies Inferred relationship Some
Neurocutaneous melanosis sequence Is a False Congenital pigmentary skin anomalies Inferred relationship Some
McCune Albright syndrome (disorder) Is a True Congenital pigmentary skin anomalies Inferred relationship Some
Birthmark Is a True Congenital pigmentary skin anomalies Inferred relationship Some
Arterial dissection and lentiginosis syndrome (disorder) Is a False Congenital pigmentary skin anomalies Inferred relationship Some

Reference Sets

Belgian GP subset (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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