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32361000119104: Congenital hemangioma (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3005269018 Congenital hemangioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3005300019 Congenital hemangioma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3005361018 Congenital haemangioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
994231000172111 hémangiome congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

13 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hemangioma Is a Hemangioma (disorder) true Inferred relationship Some
Congenital hemangioma Is a Lesion of soft tissue (disorder) false Inferred relationship Some
Congenital hemangioma Is a Mass of cardiovascular structure false Inferred relationship Some
Congenital hemangioma Is a Congenital vascular disorder (disorder) true Inferred relationship Some
Congenital hemangioma Is a Mass of soft tissue (finding) false Inferred relationship Some
Congenital hemangioma Occurrence Congenital true Inferred relationship Some 1
Congenital hemangioma Associated morphology Benign hemangioma true Inferred relationship Some 1
Congenital hemangioma Finding site Blood vessel structure (body structure) true Inferred relationship Some 1
Congenital hemangioma Is a Congenital vascular malformation (disorder) false Inferred relationship Some
Congenital hemangioma Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
Congenital hemangioma Is a Neoplasm of cardiovascular system (disorder) true Inferred relationship Some
Congenital hemangioma Is a Benign neoplasm of soft tissue (disorder) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital capillary hemangioma (disorder) Is a True Congenital hemangioma Inferred relationship Some
Rapidly involuting congenital haemangioma Is a True Congenital hemangioma Inferred relationship Some
Noninvoluting congenital hemangioma Is a True Congenital hemangioma Inferred relationship Some
angiome artérioveineux Is a False Congenital hemangioma Inferred relationship Some
A disorder defining by the association of Perineal hemangioma, External genitalia malformations, Lipomyelomeningocele, Vesicorenal abnormalities, Imperforate anus, and Skin tag. Eleven cases have been reported. Is a True Congenital hemangioma Inferred relationship Some
Primary intraosseous venous malformation is a rare, genetic vascular anomaly characterized by severe blood vessel expansion (most frequently within the craniofacial bones) with painless bone enlargement (usually of mandible, maxilla and/or orbital, nasal, and frontal bones), typically resulting in facial asymmetry and contour deformation. Midline abnormalities, such as diastasis recti, supraumbilical raphe, and hiatus hernia, are commonly associated. Additional features reported include gingival bleeding, ectopic tooth eruption, exophthalmos, loss of vision, nausea, and vomiting. Is a True Congenital hemangioma Inferred relationship Some
Mixed haemangioma Is a True Congenital hemangioma Inferred relationship Some
Verrucous hemangioma of skin Is a True Congenital hemangioma Inferred relationship Some
Maffucci syndrome Is a True Congenital hemangioma Inferred relationship Some
Cavernous hemangioma of brain (disorder) Is a True Congenital hemangioma Inferred relationship Some
Retinal racemose hemangioma Is a True Congenital hemangioma Inferred relationship Some
Hereditary neurocutaneous angiomata (disorder) Is a True Congenital hemangioma Inferred relationship Some
A rare congenital haemangioma characterised by a superficial, red to violaceous lesion with overlying telangiectasia and a surrounding pale halo, which initially behaves like a rapidly involuting congenital haemangioma, beginning to involute shortly after birth. Involution is then aborted, and a residual tumour virtually indistinguishable from non-involuting congenital haemangioma remains. This lesion grows proportionally with the child and does not regress. Is a True Congenital hemangioma Inferred relationship Some

This concept is not in any reference sets

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