86042009: Congenital melanosis (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Disorder of pigmentation (disorder)\Melanosis (disorder)\Congenital melanosis (disorder)

\Disorder of foetus and/or newborn\Congenital disease\Congenital melanosis (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

142649017 Congenital melanosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

828223014 Congenital melanosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

142649017 Congenital melanosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

142649017 Congenital melanosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

828223014 Congenital melanosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

828223014 Congenital melanosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5910431000241113 mélanose congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5910431000241113 mélanose congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital melanosis (disorder)	Is a	Congenital anomaly of integument	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital melanosis (disorder)	Associated morphology	Congenital hyperpigmentation	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital melanosis (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital melanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital melanosis (disorder)	Associated morphology	Melanosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital melanosis (disorder)	Is a	Congenital anomaly of skin (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital melanosis (disorder)	Is a	Skin lesion	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital melanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Congenital melanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Congenital melanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital melanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital melanosis (disorder)	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital melanosis (disorder)	Is a	Melanosis (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital melanosis (disorder)	Is a	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital melanosis (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital melanosis (disorder)	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital melanosis of sclera (disorder)	Is a	True	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypotrichosis with keratosis pilaris and lentiginosis	Is a	False	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Centrofacial lentiginosis syndrome	Is a	True	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary benign acanthosis nigricans with insulin resistance	Is a	True	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	True	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome	Is a	True	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial generalized lentiginosis is a rare, inherited, skin hyperpigmentation disorder characterized by widespread lentigines without associated noncutaneous abnormalities. Patients present multiple brown to dark brown, non-elevated macula of 0.2 to 1 cm in diameter, spread over the entire body, sometimes including palms or soles, but never oral mucosa.	Is a	True	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary benign acanthosis nigricans (disorder)	Is a	True	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Acromelanosis (disorder)	Is a	True	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Neurocutaneous melanosis sequence	Is a	False	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Ocular melanosis	Is a	True	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
A rare association syndrome, reported in several members of two families to date, characterized by arterial dissection, occurring at an early age and presenting with a range of manifestations depending on the vascular territory involved (headache, dysphasia, hemiparesis), in association with cystic medial necrosis and multiple lentigines (brown and black in color and mainly affecting the skin of the trunk and extremities).	Is a	True	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Nevus spilus (disorder)	Is a	False	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Neurocutaneous melanosis	Is a	False	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dermal melanocytic hamartoma (disorder)	Is a	True	Congenital melanosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets