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37095002: Lipomatosis (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
61881016 Lipomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
768921016 Lipomatosis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lipomatosis Is a Dysplasia true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Pseudolipomatous hypertrophy Is a True Lipomatosis Inferred relationship Some
Pelvic lipomatosis Is a True Lipomatosis Inferred relationship Some
Lipomatosis NEC Is a False Lipomatosis Inferred relationship Some
Lipomatosis circumscripta Associated morphology False Lipomatosis Inferred relationship Some 1
Lipomatosis renis Associated morphology False Lipomatosis Inferred relationship Some 1
Ander's disease Associated morphology False Lipomatosis Inferred relationship Some
Madelung's neck Associated morphology False Lipomatosis Inferred relationship Some
Launois-Bensaude's lipomatosis Associated morphology False Lipomatosis Inferred relationship Some 1
Nodular circumscribed lipomatosis Associated morphology False Lipomatosis Inferred relationship Some 1
Lipomatosis dolorosa Associated morphology False Lipomatosis Inferred relationship Some 1
lipomatose géante Associated morphology False Lipomatosis Inferred relationship Some 2
Launois-Bensaude's lipomatosis Associated morphology False Lipomatosis Inferred relationship Some 1
Congenital diffuse lipomatosis Associated morphology False Lipomatosis Inferred relationship Some
Encephalocraniocutaneous lipomatosis (disorder) Associated morphology False Lipomatosis Inferred relationship Some
Michelin-tyre baby Associated morphology False Lipomatosis Inferred relationship Some 3
lipomatose bénigne symétrique Associated morphology False Lipomatosis Inferred relationship Some 1
Nevus lipomatosus cutaneous superficialis Associated morphology False Lipomatosis Inferred relationship Some 2
Madelung's neck Associated morphology False Lipomatosis Inferred relationship Some 2
Lipomatous hamartoma (disorder) Associated morphology False Lipomatosis Inferred relationship Some 1
Lipomatosis (disorder) Associated morphology True Lipomatosis Inferred relationship Some 1
Fibrolipomatous hamartoma of nerve (disorder) Associated morphology False Lipomatosis Inferred relationship Some 2
Fat-storing hamartoma of dermal dendrocytes (disorder) Associated morphology False Lipomatosis Inferred relationship Some 2
Adiposis tuberosa simplex (disorder) Associated morphology False Lipomatosis Inferred relationship Some 1
Epidural lipomatosis (disorder) Associated morphology True Lipomatosis Inferred relationship Some 1
Lipomatosis circumscripta Associated morphology True Lipomatosis Inferred relationship Some 1
lipomatose bénigne symétrique Associated morphology False Lipomatosis Inferred relationship Some 1
Madelung's neck Associated morphology False Lipomatosis Inferred relationship Some 2
Lipomatosis dolorosa Associated morphology False Lipomatosis Inferred relationship Some 1
Lipomatosis renis Associated morphology True Lipomatosis Inferred relationship Some 1
Nodular circumscribed lipomatosis Associated morphology True Lipomatosis Inferred relationship Some 1
Adiposis tuberosa simplex (disorder) Associated morphology False Lipomatosis Inferred relationship Some 1
Lipomatous hypertrophy of interatrial groove Associated morphology False Lipomatosis Inferred relationship Some 1
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. Associated morphology True Lipomatosis Inferred relationship Some 1
Lipomatosis of subcutaneous tissue (disorder) Associated morphology True Lipomatosis Inferred relationship Some 1
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. Associated morphology True Lipomatosis Inferred relationship Some 2
Familial multiple lipomatosis is a rare, benign, genetic skin disease characterized by numerous, painless, encapsulated lipomas located in the subcutaneous adipose tissue of the trunk and extremities, with relative sparing of the neck and shoulders. Association with gastroduodenal lipomatosis, brain anomalies or lipomatosis, and refractory epilepsy has been reported. Associated morphology True Lipomatosis Inferred relationship Some 1
Hemihyperplasia-multiple lipomatosis syndrome is a rare, genetic overgrowth syndrome characterized by non-progressive, asymmetrical, moderate hemihyperplasia (frequently affecting the limbs) associated with slow growing, painless, multiple, recurrent, subcutaneous lipomatous masses distributed throughout entire body (in particular back, torso, extremities, fingers, axillae). Superficial vascular malformations may also be associated. Increased risk of intra-abdominal embryonal malignancies may be associated. Associated morphology True Lipomatosis Inferred relationship Some 1
A rare subcutaneous tissue disease characterised by growth of symmetric non-encapsulated masses of adipose tissue mostly around the face and neck, with variable clinical repercussions (e.g. reduced neck mobility, compression of respiratory structures). Associated morphology True Lipomatosis Inferred relationship Some 1
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. Associated morphology True Lipomatosis Inferred relationship Some 1
Congenital infiltrating lipomatosis of face (disorder) Associated morphology True Lipomatosis Inferred relationship Some 1
Perineural lipomatosis (disorder) Associated morphology True Lipomatosis Inferred relationship Some 1

This concept is not in any reference sets

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