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19928005: Fibromatosis (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
33542010 Fibromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
748582011 Fibromatosis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

10 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fibromatosis Is a Fibrosis AND/OR repair abnormality true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary camptodactyly Associated morphology False Fibromatosis Inferred relationship Some 1
Dupuytren's disease of finger Associated morphology False Fibromatosis Inferred relationship Some 1
Dupuytren's disease of palm Associated morphology False Fibromatosis Inferred relationship Some 1
Fibromatosis colli Associated morphology False Fibromatosis Inferred relationship Some 1
Dupuytren's disease of palm and finger(s), nodules with no contracture Associated morphology False Fibromatosis Inferred relationship Some 1
Dupuytren's disease of palm and finger Associated morphology False Fibromatosis Inferred relationship Some 2
Dupuytren's disease of finger, with contracture Associated morphology False Fibromatosis Inferred relationship Some 1
Fibromatosis with contracture of plantar fascia Associated morphology False Fibromatosis Inferred relationship Some 1
Dupuytren's contracture of finger (disorder) Associated morphology False Fibromatosis Inferred relationship Some 2
Cherubism with gingival fibromatosis (disorder) Associated morphology False Fibromatosis Inferred relationship Some 2
maladie de Dupuytren Associated morphology False Fibromatosis Inferred relationship Some 1
Cross syndrome Associated morphology False Fibromatosis Inferred relationship Some 1
Dupuytren's disease of palm and finger Associated morphology False Fibromatosis Inferred relationship Some 3
Dupuytren's disease of palm and finger(s), nodules with no contracture Associated morphology False Fibromatosis Inferred relationship Some 2
Dupuytren's disease of palm and finger, with contracture Associated morphology False Fibromatosis Inferred relationship Some 3
Dupuytren's disease of palm and finger, with contracture Associated morphology False Fibromatosis Inferred relationship Some 2
Gingival fibromatosis Associated morphology False Fibromatosis Inferred relationship Some 1
Plantar fascial fibromatosis Associated morphology False Fibromatosis Inferred relationship Some 1
maladie de Dupuytren Associated morphology False Fibromatosis Inferred relationship Some 1
Fibromatosis with contracture of plantar fascia Associated morphology False Fibromatosis Inferred relationship Some 6
A rare autosomal dominant disorder characterized by a generalized enlargement of the gingiva occurring at birth or during childhood that is associated with generalized hypertrichosis developing at birth, during the first years of life, or at puberty and predominantly affecting the face, upper limbs, and midback. Associated morphology True Fibromatosis Inferred relationship Some 3
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Associated morphology False Fibromatosis Inferred relationship Some 3
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. Associated morphology True Fibromatosis Inferred relationship Some 2
A rare syndrome characterized by gingival fibromatosis associated with progressive sensorineural hearing loss. It has been described in two families (with at least 16 affected members spanning five generations in one of the families, and five affected members spanning three generations in the other family). It is transmitted as an autosomal dominant trait. Associated morphology True Fibromatosis Inferred relationship Some 4
Fibromatosis (disorder) Associated morphology True Fibromatosis Inferred relationship Some 1
Dupuytren's disease of palm of bilateral hands (disorder) Associated morphology False Fibromatosis Inferred relationship Some 4
Dupuytren's disease of palm of left hand (disorder) Associated morphology False Fibromatosis Inferred relationship Some 3
Dupuytren's disease of palm of bilateral hands (disorder) Associated morphology False Fibromatosis Inferred relationship Some 3
Dupuytren's disease of palm of right hand (disorder) Associated morphology False Fibromatosis Inferred relationship Some 2
Aggressive fibromatosis (morphologic abnormality) Is a True Fibromatosis Inferred relationship Some
Cherubism with gingival fibromatosis (disorder) Associated morphology True Fibromatosis Inferred relationship Some 1
Infantile systemic hyalinosis (ISH) is a very rare disorder belonging to the heterogeneous group of genetic fibromatoses and is characterized by progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid, and adrenal glands. Associated morphology True Fibromatosis Inferred relationship Some 1
Infantile digital fibromatosis (disorder) Associated morphology False Fibromatosis Inferred relationship Some 2
A rare genetic disease characterised by infantile or childhood onset of abnormal growth of hyalinised fibrous tissue, giving rise to multiple cutaneous nodules and/or pearly papules predominantly affecting the scalp, ears, neck, face, hands, and feet. Involvement of other organs results in gingival hyperplasia, osteolytic bone lesions, and joint contractures. Some patients exhibit visceral involvement with intractable diarrhoea, increased susceptibility to infections, and severe failure to thrive. Associated morphology True Fibromatosis Inferred relationship Some 4
A rare hyaline fibromatosis syndrome with characteristics of papulo-nodular skin lesions (especially around the head and neck), soft tissue masses, gingival hypertrophy, joint contractures and osteolytic bone lesions in variable degrees. Joint contractures may cripple patients and delay normal motor development if occurring in infancy. Severe gingival hyperplasia can interfere with eating and delay dentition. Histopathology analysis of involved tissues reveals cords of spindle-shaped cells embedded in an amorphous, hyaline material. Associated morphology False Fibromatosis Inferred relationship Some 5
Sporadic camptodactyly Associated morphology True Fibromatosis Inferred relationship Some 2
Fibromatosis colli Is a True Fibromatosis Inferred relationship Some
Juvenile hyaline fibromatosis (morphologic abnormality) Is a True Fibromatosis Inferred relationship Some
Inclusion body fibromatosis Is a True Fibromatosis Inferred relationship Some

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