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1187277001: Short stature, brachydactyly, obesity, global developmental delay syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4673075011 Short stature, brachydactyly, obesity, global developmental delay syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4673076012 Short stature, brachydactyly, obesity, global developmental delay syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4673077015 SBIDDS - short stature, brachydactyly, impaired intellectual development, seizures en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399606014 A rare genetic, multiple congenital anomalies syndrome characterized by short stature, hand brachydactyly with hypoplastic distal phalanges, global development delay, intellectual disability, and more variably seizures, obesity, and craniofacial dysmorphism that includes microcephaly, high forehead, flat face, hypertelorism, deep set eyes, flat nasal bridge, averted nostrils, long philtrum, thin lip vermilion, and short neck. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399607017 A rare genetic, multiple congenital anomalies syndrome characterised by short stature, hand brachydactyly with hypoplastic distal phalanges, global development delay, intellectual disability, and more variably seizures, obesity, and craniofacial dysmorphism that includes microcephaly, high forehead, flat face, hypertelorism, deep set eyes, flat nasal bridge, averted nostrils, long philtrum, thin lip vermilion, and short neck. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4673075011 Short stature, brachydactyly, obesity, global developmental delay syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4673076012 Short stature, brachydactyly, obesity, global developmental delay syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4673077015 SBIDDS - short stature, brachydactyly, impaired intellectual development, seizures en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4673078013 A rare genetic multiple congenital anomalies syndrome with characteristics of short stature, hand brachydactyly with hypoplastic distal phalanges, global development delay, intellectual disability and more variably; seizures, obesity, and craniofacial dysmorphism that includes microcephaly, high forehead, flat face, hypertelorism, deep set eyes, flat nasal bridge, averted nostrils, long philtrum, thin lip vermilion and short neck. The malformation is due to a loss of function in the enzyme protein arginine N-methyltransferase 7 (encoded by PRMT7, 16q22.1) resulting in decreased levels of protein arginine methylation. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399606014 A rare genetic, multiple congenital anomalies syndrome characterized by short stature, hand brachydactyly with hypoplastic distal phalanges, global development delay, intellectual disability, and more variably seizures, obesity, and craniofacial dysmorphism that includes microcephaly, high forehead, flat face, hypertelorism, deep set eyes, flat nasal bridge, averted nostrils, long philtrum, thin lip vermilion, and short neck. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399607017 A rare genetic, multiple congenital anomalies syndrome characterised by short stature, hand brachydactyly with hypoplastic distal phalanges, global development delay, intellectual disability, and more variably seizures, obesity, and craniofacial dysmorphism that includes microcephaly, high forehead, flat face, hypertelorism, deep set eyes, flat nasal bridge, averted nostrils, long philtrum, thin lip vermilion, and short neck. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3417411001000116 Kleinwuchs-Brachydaktylie-Adipositas-globale Entwicklungsverzögerung-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3417411001000116 Kleinwuchs-Brachydaktylie-Adipositas-globale Entwicklungsverzögerung-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Global developmental delay true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Short stature disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Acromesomelic dysplasia group (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Finding of bone in hand true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Finding of musculoskeletal structure of digit of hand true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Brachydactyly of hand (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Congenital hypoplasia of part of upper limb true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, brachydactyly, obesity, global developmental delay syndrome Interprets Body height measure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Short stature, brachydactyly, obesity, global developmental delay syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 4
Short stature, brachydactyly, obesity, global developmental delay syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Short stature, brachydactyly, obesity, global developmental delay syndrome Finding site Entire digit of hand true Inferred relationship Existential restriction modifier (core metadata concept) 1
Short stature, brachydactyly, obesity, global developmental delay syndrome Associated morphology Abnormally short growth true Inferred relationship Existential restriction modifier (core metadata concept) 1
Short stature, brachydactyly, obesity, global developmental delay syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Short stature, brachydactyly, obesity, global developmental delay syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Short stature, brachydactyly, obesity, global developmental delay syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Short stature, brachydactyly, obesity, global developmental delay syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 2
Short stature, brachydactyly, obesity, global developmental delay syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Short stature, brachydactyly, obesity, global developmental delay syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Short stature, brachydactyly, obesity, global developmental delay syndrome Finding site Bone structure of distal phalanx of hand (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Short stature, brachydactyly, obesity, global developmental delay syndrome Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 3
Short stature, brachydactyly, obesity, global developmental delay syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Short stature, brachydactyly, obesity, global developmental delay syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Short stature, brachydactyly, obesity, global developmental delay syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Short stature, brachydactyly, obesity, global developmental delay syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 6
Short stature, brachydactyly, obesity, global developmental delay syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 6

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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