402693001: Lipomatosis (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Lipomatosis (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1770617017 Lipomatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1781793014 Lipomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

15001000077112 lipomatose 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
Lipomatosis (disorder)	Is a	Subcutaneous fat disorder	false	Inferred relationship	Some
Lipomatosis (disorder)	Finding site	Subcutaneous fatty tissue	false	Inferred relationship	Some
Lipomatosis (disorder)	Is a	Disorder of connective tissue (disorder)	false	Inferred relationship	Some
Lipomatosis (disorder)	Associated morphology	Lipomatosis	true	Inferred relationship	Some	1
Lipomatosis (disorder)	Finding site	Connective tissue structure	false	Inferred relationship	Some
Lipomatosis (disorder)	Is a	Disease	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Lipomatosis circumscripta	Is a	True	Lipomatosis (disorder)	Inferred relationship	Some
Congenital diffuse lipomatosis	Is a	False	Lipomatosis (disorder)	Inferred relationship	Some
Madelung's neck	Is a	False	Lipomatosis (disorder)	Inferred relationship	Some
Nodular circumscribed lipomatosis	Is a	False	Lipomatosis (disorder)	Inferred relationship	Some
Lipomatosis dolorosa	Is a	False	Lipomatosis (disorder)	Inferred relationship	Some
lipomatose géante	Is a	False	Lipomatosis (disorder)	Inferred relationship	Some
Adiposis tuberosa simplex (disorder)	Is a	False	Lipomatosis (disorder)	Inferred relationship	Some
Epidural lipomatosis (disorder)	Is a	True	Lipomatosis (disorder)	Inferred relationship	Some
Lipomatosis renis	Is a	True	Lipomatosis (disorder)	Inferred relationship	Some
Pseudolipomatosis hypertrophy of pancreas	Is a	True	Lipomatosis (disorder)	Inferred relationship	Some
Lipomatous hamartoma (disorder)	Is a	False	Lipomatosis (disorder)	Inferred relationship	Some
lipomatose bénigne symétrique	Is a	False	Lipomatosis (disorder)	Inferred relationship	Some
Roch-Leri mesosomatous lipomatosis is a rare benign autosomal dominant disorder of fat tissue proliferation characterized by the presence of multiple small lipomas of 2 to 5 cm in diameter in the middle third of the body (i.e. the forearms, trunk, and upper thighs), and which are generally painless and can be easily removed by local anesthesia, provided that they are not too numerous or confluent. There have been no further descriptions in the literature since 1984.	Is a	True	Lipomatosis (disorder)	Inferred relationship	Some
Lipomatosis of subcutaneous tissue (disorder)	Is a	True	Lipomatosis (disorder)	Inferred relationship	Some
A rare developmental defect during embryogenesis characterized by progressive, proportionate, asymmetric segmental overgrowth (with soft tissue hypertrophy and ballooning effect) that develops and progresses rapidly in early childhood, arteriovenous and lymphatic vascular malformations, lipomatosis and linear epidermal nevus (arranged in whorls along the lines of Blaschko). Clinical symptoms of Cowden syndrome, such as macrocephaly and progressive development of numerous hypertrophic hamartomatous and neoplastic lesions involving multiple organs and systems, are also associated. Patients present an increased risk of developing cancer.	Is a	True	Lipomatosis (disorder)	Inferred relationship	Some
A rare multiple congenital anomalies/dysmorphic syndrome characterized by axial hypotonia after birth, prolonged feeding difficulties, moderate to severe global developmental delay, seizures (in particular absence seizures), fetal digital pads, distinctive plantar fat pads anteromedial to the heels, and deep palmar and plantar grooves. Over time, fat pads may become less prominent and disappear. Distinct craniofacial dysmorphic features include a broad face with high forehead, high anterior hairline, narrow palpebral fissures that take on a crescent moon shape when smiling, broad nasal bridge and tip with anteverted nostrils, mild midfacial hypoplasia, long, smooth philtrum, thin upper lip vermillion, small, widely spaced teeth, and flat occiput/microcephaly/brachycephaly.	Is a	True	Lipomatosis (disorder)	Inferred relationship	Some
Congenital infiltrating lipomatosis of face (disorder)	Is a	True	Lipomatosis (disorder)	Inferred relationship	Some
Perineural lipomatosis (disorder)	Is a	True	Lipomatosis (disorder)	Inferred relationship	Some

This concept is not in any reference sets