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703827008: Cutaneous mastocytosis (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3009363013 Cutaneous mastocytosis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009470014 Cutaneous mastocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009363013 Cutaneous mastocytosis (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009363013 Cutaneous mastocytosis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009470014 Cutaneous mastocytosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009470014 Cutaneous mastocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cutaneous mastocytosis (morphologic abnormality) Is a Mastocytosis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)
Cutaneous mastocytosis (morphologic abnormality) Is a Hematopoietic neoplasm of uncertain behavior (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Diffuse erythrodermic mastocytosis (disorder) Associated morphology False Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Familial mastocytosis Associated morphology False Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Cutaneous mastocytosis (disorder) Associated morphology False Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Telangiectasia macularis eruptiva perstans Associated morphology False Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Diffuse cutaneous mastocytosis (morphologic abnormality) Is a True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Urticaria pigmentosa Is a False Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Solitary mastocytoma of skin (morphologic abnormality) Is a False Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
A rare multiple congenital anomalies syndrome characterized by cutaneous mastocytosis, microcephaly, microtia and/or hearing loss, hypotonia and skeletal anomalies (e.g. clinodactyly, camptodactyly, scoliosis). Additional common features are short stature, intellectual disability and difficulties. Facial dysmorphism may include upslanted palpebral fissures, highly arched palate and micrognathia. Rarely, seizures and asymmetrically small feet have been reported. Associated morphology False Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 8
A rare multiple congenital anomalies syndrome characterized by cutaneous mastocytosis, microcephaly, microtia and/or hearing loss, hypotonia and skeletal anomalies (e.g. clinodactyly, camptodactyly, scoliosis). Additional common features are short stature, intellectual disability and difficulties. Facial dysmorphism may include upslanted palpebral fissures, highly arched palate and micrognathia. Rarely, seizures and asymmetrically small feet have been reported. Associated morphology False Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Telangiectasia macularis eruptiva perstans Associated morphology False Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Diffuse erythrodermic mastocytosis (disorder) Associated morphology True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Cutaneous mastocytosis (disorder) Associated morphology True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial mastocytosis Associated morphology True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare multiple congenital anomalies syndrome characterized by cutaneous mastocytosis, microcephaly, microtia and/or hearing loss, hypotonia and skeletal anomalies (e.g. clinodactyly, camptodactyly, scoliosis). Additional common features are short stature, intellectual disability and difficulties. Facial dysmorphism may include upslanted palpebral fissures, highly arched palate and micrognathia. Rarely, seizures and asymmetrically small feet have been reported. Associated morphology False Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 6
A rare multiple congenital anomalies syndrome characterized by cutaneous mastocytosis, microcephaly, microtia and/or hearing loss, hypotonia and skeletal anomalies (e.g. clinodactyly, camptodactyly, scoliosis). Additional common features are short stature, intellectual disability and difficulties. Facial dysmorphism may include upslanted palpebral fissures, highly arched palate and micrognathia. Rarely, seizures and asymmetrically small feet have been reported. Associated morphology True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 7
Pseudoxanthomatous nodular cutaneous mastocytosis Associated morphology True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Bullous cutaneous mastocytosis Associated morphology True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Cutaneous mastocytosis, adult form Associated morphology True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Cutaneous mastocytosis, infantile form (disorder) Associated morphology True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Mastocytoma (morphologic abnormality) Is a True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cutaneous mastocytosis Associated morphology True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Maculopapular cutaneous mastocytosis (disorder) Associated morphology True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Telangiectasia macularis eruptiva perstans Associated morphology True Cutaneous mastocytosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 5

This concept is not in any reference sets

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