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770436006: Familial juvenile hypertrophy of breast (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3700855019 Familial juvenile gigantomastia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5436661018 Familial juvenile hypertrophy of breast (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5436662013 Familial juvenile hypertrophy of breast en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3700858017 A rare breast malformation disorder characterized by unilateral or bilateral, symmetrical or asymmetrical, uncontrolled, rapid and massive enlargement of the breast(s) in peripubertal females, occurring in various members of a family. Additional associated manifestations may include skin hyperemia, dilated subcutaneous veins, skin necrosis, kyphosis, lordosis and anonychia. Growth and development are otherwise normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3700859013 A rare breast malformation disorder characterised by unilateral or bilateral, symmetrical or asymmetrical, uncontrolled, rapid and massive enlargement of the breast(s) in peripubertal females, occurring in various members of a family. Additional associated manifestations may include skin hyperaemia, dilated subcutaneous veins, skin necrosis, kyphosis, lordosis and anonychia. Growth and development are otherwise normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3700855019 Familial juvenile gigantomastia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3700856018 Familial juvenile hypertrophy of the breast en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3700857010 Familial juvenile hypertrophy of the breast (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5436661018 Familial juvenile hypertrophy of breast (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5436662013 Familial juvenile hypertrophy of breast en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3700858017 A rare breast malformation disorder characterized by unilateral or bilateral, symmetrical or asymmetrical, uncontrolled, rapid and massive enlargement of the breast(s) in peripubertal females, occurring in various members of a family. Additional associated manifestations may include skin hyperemia, dilated subcutaneous veins, skin necrosis, kyphosis, lordosis and anonychia. Growth and development are otherwise normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3700859013 A rare breast malformation disorder characterised by unilateral or bilateral, symmetrical or asymmetrical, uncontrolled, rapid and massive enlargement of the breast(s) in peripubertal females, occurring in various members of a family. Additional associated manifestations may include skin hyperaemia, dilated subcutaneous veins, skin necrosis, kyphosis, lordosis and anonychia. Growth and development are otherwise normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3451501001000118 Familiäre juvenile Hypertrophie der Brust de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
926021000172115 gigantomastie juvénile familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
962241000172114 hypertrophie mammaire juvénile familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
926021000172115 gigantomastie juvénile familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
962241000172114 hypertrophie mammaire juvénile familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3451501001000118 Familiäre juvenile Hypertrophie der Brust de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare breast malformation disorder characterized by unilateral or bilateral, symmetrical or asymmetrical, uncontrolled, rapid and massive enlargement of the breast(s) in peripubertal females, occurring in various members of a family. Additional associated manifestations may include skin hyperemia, dilated subcutaneous veins, skin necrosis, kyphosis, lordosis and anonychia. Growth and development are otherwise normal. Occurrence Childhood true Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare breast malformation disorder characterized by unilateral or bilateral, symmetrical or asymmetrical, uncontrolled, rapid and massive enlargement of the breast(s) in peripubertal females, occurring in various members of a family. Additional associated manifestations may include skin hyperemia, dilated subcutaneous veins, skin necrosis, kyphosis, lordosis and anonychia. Growth and development are otherwise normal. Is a Hereditary disorder by system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
A rare breast malformation disorder characterized by unilateral or bilateral, symmetrical or asymmetrical, uncontrolled, rapid and massive enlargement of the breast(s) in peripubertal females, occurring in various members of a family. Additional associated manifestations may include skin hyperemia, dilated subcutaneous veins, skin necrosis, kyphosis, lordosis and anonychia. Growth and development are otherwise normal. Finding site Entire breast true Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare breast malformation disorder characterized by unilateral or bilateral, symmetrical or asymmetrical, uncontrolled, rapid and massive enlargement of the breast(s) in peripubertal females, occurring in various members of a family. Additional associated manifestations may include skin hyperemia, dilated subcutaneous veins, skin necrosis, kyphosis, lordosis and anonychia. Growth and development are otherwise normal. Associated morphology Giant hypertrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare breast malformation disorder characterized by unilateral or bilateral, symmetrical or asymmetrical, uncontrolled, rapid and massive enlargement of the breast(s) in peripubertal females, occurring in various members of a family. Additional associated manifestations may include skin hyperemia, dilated subcutaneous veins, skin necrosis, kyphosis, lordosis and anonychia. Growth and development are otherwise normal. Is a Gigantomastia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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