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32570371000036100: Neoplasm and/or hamartoma reference set (foundation metadata concept)


Status: current, Primitive. Date: 31-May 2012. Module: SNOMED Clinical Terms Australian extension

Descriptions:

Id Description Lang Type Status Case? Module
108643281000036112 Neoplasm and/or hamartoma reference set en Synonym Active Case insensitive SNOMED Clinical Terms Australian extension
108643291000036114 Neoplasm and/or hamartoma reference set (foundation metadata concept) en Fully specified name Active Case insensitive SNOMED Clinical Terms Australian extension
4351181000168110 <p>Supports the recording of neoplasm and/or hamartoma findings in Australian e-health settings. This reference set has been derived from the <em>Clinical finding foundation reference set.</em></p><p>This reference set can be used:<ul><li>Within implementations where use-case specific reference sets for neoplasm and/or hamartomas are yet to be developed.</li><li>As the basis for developing further use-case specific reference sets for neoplasm and/or hamartomas, through a process of constraint.</li><li>As a benchmark, against which use-case specific reference sets that have been developed by the SNOMED CT-AU user community can be tested to assure that they are logical constraints of content relating to neoplasms and/or hamartomas.</li></ul></p><p><b>Target client: </b>Australian e-health clinical information systems, for example, within Oncology groups.</p> en Definition Active Case sensitive SNOMED Clinical Terms Australian extension


10098 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neoplasm and/or hamartoma reference set Developed by Australian Digital Health Agency true Inferred relationship Some 348630873
Neoplasm and/or hamartoma reference set Has licence SNOMED CT-AU licence​ true Inferred relationship Some 1097591398
Neoplasm and/or hamartoma reference set Is a Clinical finding foundation reference set false Inferred relationship Some
Neoplasm and/or hamartoma reference set Is a Oncology clinical group true Inferred relationship Some
Neoplasm and/or hamartoma reference set Is a Attribute value type false Inferred relationship Some
Neoplasm and/or hamartoma reference set Is a Simple type reference set true Inferred relationship Some

Members
Congenital accessory skin tag
Congenital benign giant pigmented naevus of skin
Congenital capillary haemangioma
Congenital cutaneous angiomatosis
Congenital diffuse lipomatosis
Congenital epignathus
Congenital erector pili hamartoma
Congenital hamartoma
Bilateral congenital hamartoma of irises
Congenital hamartoma of skin
Congenital haemangioma
Congenital intermediate sized melanocytic naevus
Congenital leptomeningeal angiomatosis
CLOVES syndrome
Congenital lymphangioma
Congenital lymphangioma of larynx
Congenital malignant melanoma
Congenital melanocytic naevus of face
Congenital melanocytic naevus of trunk
Congenital panfollicular naevus
Congenital pigmented melanocytic naevus
Congenital pigmented melanocytic naevus of skin
Congenital pigmented melanocytic naevus of skin of left ear
Congenital pigmented melanocytic naevus of skin of left lower limb
Congenital pigmented melanocytic naevus of skin of left upper limb
Congenital pigmented melanocytic naevus of skin of lip
Congenital pigmented melanocytic naevus of skin of neck
Congenital pigmented melanocytic naevus of skin of right ear
Congenital pigmented melanocytic naevus of skin of right lower limb
Congenital pigmented melanocytic naevus of skin of right upper limb
Congenital pigmented melanocytic naevus of skin of scalp
Congenital pigmented naevus with atypical melanocytic proliferation
Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome
Retinal racemose haemangioma
Congenital rhabdomyoma of heart
Congenital rhabdomyomatous mesenchymal hamartoma
Congenital small melanocytic naevus
Congenital nasopharyngeal teratoma
Conjunctival cystoid naevus
Conjunctival intraepithelial neoplasia
Connective tissue naevus of skin
Core binding factor acute myeloid leukaemia
Corneal intraepithelial neoplasia
Cortical adenoma of kidney
Corticotroph adenoma
Cowden syndrome
Craniopharyngioma
Cutaneous fibrosarcoma
Cutaneous leiomyoma
Cutaneous leiomyosarcoma
Cutaneous leiomyosarcoma with granular cell change
Cutaneous lymphadenoma
Cutaneous mastocytosis
Hennekam Beemer syndrome
Cutaneous meningioma
Cutaneous neurofibroma
Cutaneous neuroma
Cutaneous papilloma of breast
Cutaneous papilloma of nipple
Cutaneous papillomatosis
Cutaneous reticulohistiocytosis
Cutaneous storiform neurofibroma
Cutaneous/peripheral T-cell lymphoma
Cystadenocarcinoma of kidney
Cystadenocarcinoma of oropharynx
Cystadenocarcinoma of ovary
Cystadenocarcinoma of pancreas
Cystadenoma of kidney
Hepatic cystadenoma
Cystadenoma of ovary in childhood
Cystadenoma of pancreas
Cystic basal cell carcinoma
Cystic hamartoma of lung and kidney
Cystic hygroma
Cystic hygroma in fetus
Cystic hygroma in fetus with hydrops
Cystic mesothelioma of peritoneum
Cystic partially differentiated nephroblastoma of kidney
Cystic renal cell carcinoma of kidney
Cystic trichoblastoma
Bilateral cystoid naevus of conjunctiva of eyes
Cystoid naevus of conjunctiva of left eye
Cystoid naevus of conjunctiva of right eye
Dartoic myoma
Dedifferentiated liposarcoma
Deep penetrating melanocytic naevus
Deep subfascial lipoma
Degeneration of uterine fibroid
Delta heavy chain disease
Dendritic cell neoplasm
Dendritic cell sarcoma
Dermal cellular naevus
Dermal melanocytic hamartoma
Dermal nerve sheath myxoma
Dermal nerve sheath myxoma, cellular
Dermatofibroma
Bilateral dermatofibroma of lower limbs
Bilateral dermatofibroma of upper limbs
Dermatofibroma of left lower limb
Dermatofibroma of left upper limb
Dermatofibroma of neck

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