717813005: Global developmental delay, osteopenia, ectodermal defect syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Global developmental delay, osteopenia, ectodermal defect syndrome
\Musculoskeletal finding\Bone finding\Disorder of bone\Degenerative disorder of bone\Osteopenia\Global developmental delay, osteopenia, ectodermal defect syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Degenerative disorder of musculoskeletal system\Degenerative disorder of bone\Osteopenia\Global developmental delay, osteopenia, ectodermal defect syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Global developmental delay, osteopenia, ectodermal defect syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Degenerative disorder of bone\Osteopenia\Global developmental delay, osteopenia, ectodermal defect syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Global developmental delay, osteopenia, ectodermal defect syndrome

\Disease\Disorder of embryonic structure\Congenital ectodermal defect\Global developmental delay, osteopenia, ectodermal defect syndrome
\Disease\Degenerative disorder\Degenerative disorder of musculoskeletal system\Degenerative disorder of bone\Osteopenia\Global developmental delay, osteopenia, ectodermal defect syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Degenerative disorder of musculoskeletal system\Degenerative disorder of bone\Osteopenia\Global developmental delay, osteopenia, ectodermal defect syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Global developmental delay, osteopenia, ectodermal defect syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Degenerative disorder of bone\Osteopenia\Global developmental delay, osteopenia, ectodermal defect syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Global developmental delay, osteopenia, ectodermal defect syndrome
\Disease\Congenital disease\Congenital malformation\Congenital ectodermal defect\Global developmental delay, osteopenia, ectodermal defect syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Global developmental delay, osteopenia, ectodermal defect syndrome
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Global developmental delay, osteopenia, ectodermal defect syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital ectodermal defect\Global developmental delay, osteopenia, ectodermal defect syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Global developmental delay, osteopenia, ectodermal defect syndrome
\Disease\Developmental disorder\Developmental delay\Global developmental delay\Global developmental delay, osteopenia, ectodermal defect syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3323604010 Global developmental delay, osteopenia, ectodermal defect syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3323605011 Global developmental delay, osteopenia, ectodermal defect syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Global developmental delay, osteopenia, ectodermal defect syndrome	Is a	Global developmental delay	true	Inferred relationship	Existential restriction modifier
Global developmental delay, osteopenia, ectodermal defect syndrome	Is a	Congenital ectodermal defect	true	Inferred relationship	Existential restriction modifier
Global developmental delay, osteopenia, ectodermal defect syndrome	Is a	Osteopenia	true	Inferred relationship	Existential restriction modifier
Global developmental delay, osteopenia, ectodermal defect syndrome	Is a	Congenital connective tissue disorder	false	Inferred relationship	Existential restriction modifier
Global developmental delay, osteopenia, ectodermal defect syndrome	Associated morphology	Osteopenia	false	Inferred relationship	Existential restriction modifier	2
Global developmental delay, osteopenia, ectodermal defect syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Global developmental delay, osteopenia, ectodermal defect syndrome	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	2
Global developmental delay, osteopenia, ectodermal defect syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	3
Global developmental delay, osteopenia, ectodermal defect syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Global developmental delay, osteopenia, ectodermal defect syndrome	Finding site	Ectoderm structure	false	Inferred relationship	Existential restriction modifier	3
Global developmental delay, osteopenia, ectodermal defect syndrome	Finding site	Ectoderm structure	true	Inferred relationship	Existential restriction modifier	2
Global developmental delay, osteopenia, ectodermal defect syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Global developmental delay, osteopenia, ectodermal defect syndrome	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Existential restriction modifier
Global developmental delay, osteopenia, ectodermal defect syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Global developmental delay, osteopenia, ectodermal defect syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Global developmental delay, osteopenia, ectodermal defect syndrome	Associated morphology	Osteopenia	true	Inferred relationship	Existential restriction modifier	1
Global developmental delay, osteopenia, ectodermal defect syndrome	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Global developmental delay, osteopenia, ectodermal defect syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3323604010	Global developmental delay, osteopenia, ectodermal defect syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3323605011	Global developmental delay, osteopenia, ectodermal defect syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module