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205564003: Congenital pigmentary skin anomalies (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
315243010 Congenital pigmentary skin anomalies en Synonym Active Entire term case insensitive SNOMED CT core module
590950015 Congenital pigmentary skin anomalies (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2475672012 Congenital pigmentary anomaly of skin en Synonym Active Entire term case insensitive SNOMED CT core module

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 Existential restriction modifier
Congenital pigmentary skin anomalies Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier
Congenital pigmentary skin anomalies Is a Congenital heart disease false Inferred relationship Existential restriction modifier
Congenital pigmentary skin anomalies Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomalies Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Congenital pigmentary skin anomalies Finding site Jaw region structure false Inferred relationship Existential restriction modifier
Congenital pigmentary skin anomalies Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomalies Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital pigmentary skin anomalies Finding site Upper gastrointestinal tract structure false Inferred relationship Existential restriction modifier
Congenital pigmentary skin anomalies Finding site Heart structure false Inferred relationship Existential restriction modifier
Congenital pigmentary skin anomalies Finding site Tongue structure false Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomalies Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomalies Finding site Structure of cardiovascular system subdivision false Inferred relationship Existential restriction modifier 2
Congenital pigmentary skin anomalies Is a Congenital anomaly of skin true Inferred relationship Existential restriction modifier
Congenital pigmentary skin anomalies Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier
Congenital pigmentary skin anomalies Is a Disorder of skin pigmentation true Inferred relationship Existential restriction modifier
Congenital pigmentary skin anomalies Associated morphology Pigment alteration false Inferred relationship Existential restriction modifier 2
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Congenital pigmentary skin anomalies Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Congenital pigmentary skin anomalies Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Congenital pigmentary skin anomalies Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Congenital pigmentary skin anomalies Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomalies Associated morphology Pigment alteration true Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomalies Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomalies Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital pigmentary skin anomaly NOS Is a False Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Congenital deficiency of pigment of skin Is a True Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Terminal osseous dysplasia and pigmentary defect syndrome Is a False Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Neuroectodermal melanolysosomal disease Is a True Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome Is a True Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Carney complex Is a True Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Familial progressive hyperpigmentation and hypopigmentation of skin Is a True Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Carney complex, trismus, pseudocamptodactyly syndrome Is a True Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Hereditary benign acanthosis nigricans Is a False Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Hereditary benign acanthosis nigricans with insulin resistance Is a False Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Hypotrichosis with keratosis pilaris and lentiginosis Is a False Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Peutz-Jeghers syndrome Is a False Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Familial generalized lentiginosis Is a True Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a False Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Inherited cutaneous hyperpigmentation Is a True Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Pseudoleprechaunism syndrome Patterson type Is a True Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Neurocutaneous melanosis sequence Is a False Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
McCune Albright syndrome Is a True Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Birthmark Is a True Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Arterial dissection and lentiginosis syndrome Is a False Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier
Congenital pigmentary skin anomaly NOS Is a False Congenital pigmentary skin anomalies Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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