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400083002: Congenital hamartoma of skin (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1768003013 Congenital hamartoma of skin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1779349016 Congenital hamartoma of skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1768003013 Congenital hamartoma of skin (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1768003013 Congenital hamartoma of skin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1779349016 Congenital hamartoma of skin en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1779349016 Congenital hamartoma of skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5258141000241117 harmatome congénital de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5258141000241117 harmatome congénital de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

21 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hamartoma of skin (disorder) Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma of skin (disorder) Is a Hamartoma of skin (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma of skin (disorder) Is a Congenital hamartoma (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma of skin (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hamartoma of skin (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma of skin (disorder) Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hamartoma of skin (disorder) Associated morphology Hamartoma true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hamartoma of skin (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hamartoma of skin (disorder) Is a Congenital anomaly of skin (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma of skin (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hamartoma of skin (disorder) Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hamartoma of skin (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hamartoma of skin (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hamartoma of skin (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hamartoma of skin (disorder) Is a Disorder involving the integument of fetus OR newborn true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital absence of skin on scalp with epidermal nevi Is a False Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Shagreen patch Is a False Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pigmented melanocytic nevus of skin (disorder) Is a False Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital erector pili hamartoma Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Malignant melanoma arising in congenital nevus Is a False Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital melanocytic nevus of skin of face (disorder) Is a False Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
PTEN hamartoma tumour syndrome Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital melanocytic nevus of trunk (disorder) Is a False Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypotrichosis with keratosis pilaris and lentiginosis Is a False Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome Is a False Congenital hamartoma of skin (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 hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Centrofacial lentiginosis syndrome Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital panfollicular nevus Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare skin disease characterised by the association of sebaceous naevus and aplasia cutis congenita (usually on the scalp and face) in conjunction with limbal dermoid of the eye, a giant congenital melanocytic naevus and variable central nervous system abnormalities including seizures, hydrocephalus, neurocutaneous melanosis, arachnoid cysts, and diffuse unilateral hemisphere enlargement. Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Didymosis aplasticosebacea (disorder) Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hair follicle nevus Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Nevus comedonicus Is a True Congenital hamartoma of skin (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 hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Proteus syndrome Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Linear basal cell nevus Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Nevus spilus (disorder) Is a False Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
CLOVE syndrome Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Papular epidermal naevi with skyline basal cell layers syndrome Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dermal melanocytic hamartoma (disorder) Is a True Congenital hamartoma of skin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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