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78572006: Neurocutaneous syndrome (disorder)


Status: current, Not 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
130379012 Neuroectodermal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
130382019 Neurocutaneous syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
130383012 Phacomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
130384018 Phakomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
819527015 Neurocutaneous syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1234270011 Phakomatoses en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4646731000241116 dysplasie neuro-ectodermique congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


39 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neurocutaneous syndrome Is a Skin lesion false Inferred relationship Some
Neurocutaneous syndrome Is a Neoplastic disease false Inferred relationship Some
Neurocutaneous syndrome Is a Hereditary disorder of nervous system false Inferred relationship Some
Neurocutaneous syndrome Is a Congenital anomaly of skin false Inferred relationship Some
Neurocutaneous syndrome Is a Hereditary disorder of the integument false Inferred relationship Some
Neurocutaneous syndrome Occurrence Congenital false Inferred relationship Some
Neurocutaneous syndrome Finding site Structure of nervous system (body structure) false Inferred relationship Some 1
Neurocutaneous syndrome Finding site Structure of skin region false Inferred relationship Some 1
Neurocutaneous syndrome Associated morphology Neoplasm false Inferred relationship Some
Neurocutaneous syndrome Associated morphology Dysplasia false Inferred relationship Some 1
Neurocutaneous syndrome Associated morphology anomalie congénitale false Inferred relationship Some 1
Neurocutaneous syndrome Is a Site-specific disorder of skin false Inferred relationship Some
Neurocutaneous syndrome Associated morphology anomalie congénitale false Inferred relationship Some 2
Neurocutaneous syndrome Is a Congenital anomaly of nervous system false Inferred relationship Some
Neurocutaneous syndrome Finding site Skin structure false Inferred relationship Some 1
Neurocutaneous syndrome Associated morphology anomalie congénitale false Inferred relationship Some 1
Neurocutaneous syndrome Associated morphology anomalie congénitale false Inferred relationship Some 2
Neurocutaneous syndrome Associated morphology anomalie congénitale false Inferred relationship Some 1
Neurocutaneous syndrome Associated morphology anomalie congénitale false Inferred relationship Some 2
Neurocutaneous syndrome Finding site Structure of nervous system (body structure) true Inferred relationship Some 1
Neurocutaneous syndrome Finding site Skin structure false Inferred relationship Some 1
Neurocutaneous syndrome Associated morphology anomalie congénitale false Inferred relationship Some 1
Neurocutaneous syndrome Occurrence Congenital true Inferred relationship Some 2
Neurocutaneous syndrome Associated morphology anomalie du développement false Inferred relationship Some 2
Neurocutaneous syndrome Occurrence Congenital false Inferred relationship Some 3
Neurocutaneous syndrome Associated morphology anomalie du développement false Inferred relationship Some 3
Neurocutaneous syndrome Finding site Structure of nervous system (body structure) false Inferred relationship Some 2
Neurocutaneous syndrome Finding site Skin structure false Inferred relationship Some 3
Neurocutaneous syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Some 2
Neurocutaneous syndrome Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
Neurocutaneous syndrome Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
Neurocutaneous syndrome Occurrence Congenital true Inferred relationship Some 1
Neurocutaneous syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
Neurocutaneous syndrome Is a Neoplasm of nervous system true Inferred relationship Some
Neurocutaneous syndrome Is a Congenital disease true Inferred relationship Some
Neurocutaneous syndrome Is a Neoplasm of skin true Inferred relationship Some
Neurocutaneous syndrome Associated morphology Neoplasm true Inferred relationship Some 1
Neurocutaneous syndrome Finding site Skin structure true Inferred relationship Some 2
Neurocutaneous syndrome Associated morphology Neoplasm true Inferred relationship Some 2
Neurocutaneous syndrome Is a Fetal and/or neonatal disorder of integument true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Neurofibromatosis syndrome Is a True Neurocutaneous syndrome Inferred relationship Some
Sturge-Weber syndrome Is a True Neurocutaneous syndrome Inferred relationship Some
Von Hippel-Lindau syndrome Is a True Neurocutaneous syndrome Inferred relationship Some
Peutz-Jeghers syndrome Is a True Neurocutaneous syndrome Inferred relationship Some
Tuberous sclerosis syndrome Is a True Neurocutaneous syndrome Inferred relationship Some
[X]Other phakomatoses, not elsewhere classified Is a False Neurocutaneous syndrome Inferred relationship Some
Vascular neurocutaneous syndrome Is a True Neurocutaneous syndrome Inferred relationship Some
Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome (disorder) Is a False Neurocutaneous syndrome Inferred relationship Some
syndrome de malformations de la fosse postérieure, hémangiomes capillaires, anomalies de l'anatomie des artères cérébrales, coarctation de l'aorte et autres malformations cardiaques, anomalies oculaires et anomalies sternales Is a False Neurocutaneous syndrome Inferred relationship Some
Phakomatosis cesioflammea Is a True Neurocutaneous syndrome Inferred relationship Some
Phakomatosis spilorosea Is a True Neurocutaneous syndrome Inferred relationship Some
Phakomatosis caesiomarmorata Is a True Neurocutaneous syndrome Inferred relationship Some
Cerebral-retinal arteriovenous aneurysm (disorder) Is a True Neurocutaneous syndrome Inferred relationship Some
A rare, genetic, neurocutaneous disease characterized by severe developmental abnormalities of the nervous system and aberrant differentiation of the epidermis. Patients present with a unique constellation of clinical signs described with the acronym CEDNIK: CErebral Dysgenesis, Neuropathy, Ichthyosis, and palmoplantar Keratoderma. Is a True Neurocutaneous syndrome Inferred relationship Some
A rare neurocutaneous syndrome characterized by the association of cerebellum (rhombencephalosynapsis), cranial nerves (trigeminal anesthesia), and scalp (alopecia) abnormalities. Other features observed in patients were craniosynostosis, midfacial hypoplasia, bilateral corneal opacities, low-set ears, short stature, moderate intellectual impairment and ataxia. Hyperactivity, depression, self-injurious behavior and bipolar disorder have also been reported. Is a True Neurocutaneous syndrome Inferred relationship Some
A rare genetic neurological disease characterized by silvery hair, profound dysfunction of central nervous system, abnormal melanocytes and melanosomes and abnormal inclusion bodies in fibroblast and other cells. Is a True Neurocutaneous syndrome Inferred relationship Some
Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome is a rare, genetic pigmentation anomaly of the skin disorder characterized by congenital hypomelanotic and hypermelanotic cutaneous macules associated with, in some patients, retarded growth and intellectual disability. There have been no further descriptions in the literature since 1978. Is a True Neurocutaneous syndrome Inferred relationship Some
PENS syndrome is a rare, genetic, neurocutaneous syndrome characterized by the presence of randomly distributed, small, white to yellowish, multiple, rounded or irregular polycyclically-shaped, epidermal keratotic papules and plaques of gem-like appearance with a rough surface, typically located on the trunk and proximal limbs, associated with variable neurological abnormalities, including psychomotor delay, epilepsy, speech and language impairment and attention deficit-hyperactivity disorder. Clumsiness, dyslexia and ophthalmological abnormalities have also been reported. Is a True Neurocutaneous syndrome Inferred relationship Some
A rare complex overgrowth syndrome characterised by progressive overgrowth of the skeleton, skin, adipose, and central nervous systems. Is a True Neurocutaneous syndrome Inferred relationship Some

Reference Sets

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