1169362009: Overgrowth syndrome with 2q37 translocation (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Body measurement finding\Height / growth finding\General finding of height\Disorder of stature\Overgrowth syndrome with 2q37 translocation
• \Finding of general physiological development\Disorder of stature\Overgrowth syndrome with 2q37 translocation
• \Musculoskeletal finding\Disorder of musculoskeletal system\...
• \Disorder of skeletal system\Overgrowth syndrome with 2q37 translocation
• \Congenital anomaly of musculoskeletal system\Overgrowth syndrome with 2q37 translocation
• \Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Multiple malformation syndrome with early overgrowth\Overgrowth syndrome with 2q37 translocation
• \Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Overgrowth syndrome with 2q37 translocation
• \Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 2\Overgrowth syndrome with 2q37 translocation
• \Disease\Chromosomal disorder (disorder)\Autosomal chromosomal disorder (disorder)\Autosomal translocation\Overgrowth syndrome with 2q37 translocation
• \Disease\Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 2\Overgrowth syndrome with 2q37 translocation
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Overgrowth syndrome with 2q37 translocation
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Overgrowth syndrome with 2q37 translocation
• \Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Multiple malformation syndrome with early overgrowth\Overgrowth syndrome with 2q37 translocation
• \Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Overgrowth syndrome with 2q37 translocation
• \Disease\Developmental disorder\Disorder of stature\Overgrowth syndrome with 2q37 translocation

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4607808019	Overgrowth syndrome with 2q37 translocation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4607809010	Overgrowth syndrome with 2q37 translocation (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5399314013	A rare overgrowth syndrome with skeletal involvement characterized by long and slim body habitus and multiple skeletal manifestations, such as scoliosis, macrodactyly of the big toes, arachnodactyly of fingers and toes, camptodactyly and clinodactyly, and progressive valgus deformities of the feet. Epimetaphyseal dysplasia, bowing of the tibiae, and dysmorphic facial features (hypertelorism, high palate, or micrognathia), as well as aortic root dilatation and umbilical hernia have also been reported.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5399315014	A rare overgrowth syndrome with skeletal involvement characterised by long and slim body habitus and multiple skeletal manifestations, such as scoliosis, macrodactyly of the big toes, arachnodactyly of fingers and toes, camptodactyly and clinodactyly, and progressive valgus deformities of the feet. Epimetaphyseal dysplasia, bowing of the tibiae, and dysmorphic facial features (hypertelorism, high palate, or micrognathia), as well as aortic root dilatation and umbilical hernia have also been reported.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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