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254154003: Congenital ectodermal defect (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2015. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
378332019 Congenital ectodermal defect en Synonym Active Entire term case insensitive SNOMED CT core module
645006015 Congenital ectodermal defect (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

259 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital ectodermal defect Is a Congenital anomaly of skin false Inferred relationship Existential restriction modifier
Congenital ectodermal defect Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Congenital ectodermal defect Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital ectodermal defect Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital ectodermal defect Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Congenital ectodermal defect Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital ectodermal defect Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Congenital ectodermal defect Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital ectodermal defect Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Congenital ectodermal defect Is a Congenital malformation true Inferred relationship Existential restriction modifier
Congenital ectodermal defect Is a Disorder of embryonic structure true Inferred relationship Existential restriction modifier
Congenital ectodermal defect Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital ectodermal defect Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Congenital ectodermal defect Finding site Ectoderm structure true Inferred relationship Existential restriction modifier 1
Congenital ectodermal defect Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital ectodermal defect Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Ectodermal dysplasia Is a True Congenital ectodermal defect Inferred relationship Existential restriction modifier
Neural tube defect Is a True Congenital ectodermal defect Inferred relationship Existential restriction modifier
Global developmental delay, osteopenia, ectodermal defect syndrome Is a True Congenital ectodermal defect Inferred relationship Existential restriction modifier
Neuroectodermal endocrine syndrome Is a False Congenital ectodermal defect Inferred relationship Existential restriction modifier
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome Is a True Congenital ectodermal defect Inferred relationship Existential restriction modifier
Autosomal dominant palmoplantar keratoderma and congenital alopecia Is a True Congenital ectodermal defect Inferred relationship Existential restriction modifier
Scalp, ear, nipple syndrome Is a False Congenital ectodermal defect Inferred relationship Existential restriction modifier
Hypotrichosis with juvenile macular degeneration syndrome Is a False Congenital ectodermal defect Inferred relationship Existential restriction modifier
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome Is a True Congenital ectodermal defect Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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