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363185004: Hereditary disorder of the integument (disorder)

Status: current, 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
482325014 Hereditary disorder of the integument en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
754981012 Hereditary disorder of the integument (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

659 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary disorder of the integument Is a Hereditary disorder by system true Inferred relationship Some
Hereditary disorder of the integument Is a Disorder of integument true Inferred relationship Some
Hereditary disorder of the integument Finding site Structure of integumentary system (body structure) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Carney complex (disorder) Is a False Hereditary disorder of the integument Inferred relationship Some
Gastrocutaneous syndrome Is a True Hereditary disorder of the integument Inferred relationship Some
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) Is a True Hereditary disorder of the integument Inferred relationship Some
Inherited cutaneous hyperpigmentation Is a True Hereditary disorder of the integument Inferred relationship Some
Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome Is a True Hereditary disorder of the integument Inferred relationship Some
Neurofibromatosis type 6 Is a True Hereditary disorder of the integument Inferred relationship Some
Hereditary distal onycholysis Is a True Hereditary disorder of the integument Inferred relationship Some
Congenital isolated onychodysplasia Is a True Hereditary disorder of the integument Inferred relationship Some
Birt Hogg Dubé syndrome Is a True Hereditary disorder of the integument Inferred relationship Some
Congenital insensitivity to pain, hyperhidrosis, absence of cutaneous sensory innervation (disorder) Is a True Hereditary disorder of the integument Inferred relationship Some
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) Is a True Hereditary disorder of the integument Inferred relationship Some
Full schwannomatosis Is a True Hereditary disorder of the integument Inferred relationship Some
Autosomal recessive hyper-IgE syndrome due to ZNF341 deficiency Is a True Hereditary disorder of the integument Inferred relationship Some
Coagulation factor XII-associated cold autoinflammatory syndrome (disorder) Is a True Hereditary disorder of the integument Inferred relationship Some
Caspase recruitment domain family member 11-associated atopy with dominant interference of nuclear factor kappa-B signaling syndrome (disorder) Is a True Hereditary disorder of the integument Inferred relationship Some
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation Is a True Hereditary disorder of the integument Inferred relationship Some
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB gain of function mutation (disorder) Is a True Hereditary disorder of the integument Inferred relationship Some

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