900000000000526001: REPLACED BY association reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Association type\Historical association reference set (foundation metadata concept)\REPLACED BY association reference set (foundation metadata concept)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT model component module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

900000000001156010 REPLACED BY association reference set (foundation metadata concept) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

900000000001157018 REPLACED BY association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
REPLACED BY association reference set (foundation metadata concept)	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
Falcivibrio species	Mobiluncus
Falcivibrio vaginalis	Mobiluncus curtisii
Fall from or out of building or other structure	Fall from building
Fall from or out of building or other structure	Fall from building
Fall from or out of building or other structure NOS	Fall from building
Fall into hole or other opening in surface	Fall into hole
Fall into hole or other opening in surface	Fall into hole
Fall into other hole or other opening in surface	Fall into hole
Fallopian insufflation NOS	Inflation of fallopian tube
Fallopian insufflation NOS	Inflation of fallopian tube
Fallopian tube TNM finding	American Joint Committee on Cancer allowable value
Familial alobar holoprosencephaly	Holoprosencephaly sequence
Familial amyloid neuropathy, Finnish type	A rare, systemic amyloidosis characterized by a triad of ophthalmologic, neurologic and dermatologic findings due to the deposition of gelsolin amyloid fibrils in these tissues. Clinical manifestations include corneal lattice dystrophy, cranial neuropathy, especially affecting the facial nerve, bulbar signs, cutis laxa, increased skin fragility, and less commonly peripheral neuropathy and renal failure.
Familial glomus tumor of skin	Familial benign glomus tumour of skin
Familial lambdoid synostosis	Nonsyndromic premature fusion of a single suture.
Familial lobular glomerulopathy	A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life.
Familial multiple café-au-lait macules without neurofibromatosis	Neurofibromatosis type 6 (NF6), also referred as café-au-lait spots syndrome, is a cutaneous disorder characterized by the presence of several café-au-lait (CAL) macules without any other manifestations of neurofibromatosis or any other systemic disorder.
Familial multiple fibrofolliculoma	Multiple fibrofolliculomas
Familial neonatal seizures	A familial type of self-limited focal epilepsy with onset typically between day two and seven of life. Seizures are focal tonic at onset, affecting the head, face, and limbs. Focal clonic or tonic seizures may evolve to bilateral tonic or clonic seizures. Onset may alternate between hemispheres. Autonomic features (apnea and cyanosis) can be seen. Seizure semiology may progress in a sequential pattern with tonic, clonic, myoclonic and autonomic features following each other without a single predominant feature. Clusters of seizures can occur over hours or days with the neonate behaving normally between events. Developmental progress is usually normal. The electroencephalogram (EEG) background is normal or has minor nonspecific abnormalities. Focal interictal epileptiform abnormalities can be seen in the central, centrotemporal or frontotemporal regions. MRI is normal or has nonspecific findings. Pathogenic variants are seen in KCNQ2, KCNQ3 and SCN2A.
Familiar environment	Familiar environment (finding)
Families muridae AND/OR gliridae	Family Muridae (organism)
Family Aceraceae	Soapberries
Family Aceraceae poisoning	Sapindaceae poisoning (disorder)
Family Acidaminococcaceae	Family Veillonellaceae (organism)
Family Archiangiaceae	Family Archangiaceae (organism)
Family Aspersentidae	Family Heteracanthocephalidae (organism)
Family Azotobacteraceae	Subfamily Azobacter group (organism)
Family Beggiatoaceae	Family Thiotrichaceae (organism)
Family Catamblyrhynchidae	Family Thraupidae (organism)
Family Caulobacteriaceae	Family Caulobacteraceae (organism)
Family Chamaeidae	Family Sylviidae (organism)
Family Dendrocolaptidae	Family Furnariidae (organism)
Family Dendrocygnidae	Subfamily Dendrocygninae (organism)
Family Fimbriariidae	Family Fimbriidae
Family Hippocastanaceae - horsechesnut	Soapberries
Family Myoobiidae	Family Myobiidae (organism)
Family Phytotomidae	Subfamily Phytotominae (organism)
Family Planococaceae	Family Planococcaceae (organism)
Family Pseudoacanthocephalidae	Family Echinorhynchidae (organism)
Family Rhiziobiaceae	Family Rhizobiaceae (organism)
Family Streblidae - bat fly	Subfamily Streblinae (organism)
Family Thysanosomidae	Subfamily Thysanosomatinae
Family Veillonaceae	Family Veillonellaceae (organism)
Family Zapodidae	Family Dipodidae (organism)
Family apoidea - bee	Bee (organism)
Family atelopodidae	Family Bufonidae
Family balaenicipitidae	Family Pelecanidae (organism)
Family cacatuidae	Family Psittacidae (organism)
Family capitonidae	Subfamily Capitoninae (organism)
Family cathartidae	Family Ciconiidae (organism)
Family chironomidae - midge	Midge
Family circumstance NOS	Details of family - finding
Family circumstance NOS	Details of family - finding
Family circumstance NOS	Details of family - finding
Family cochleariidae	Family Ardeidae (organism)
Family cricetidae AND/OR other rat	Genus Rattus (organism)
Family crotalidae - crotalid	Subfamily Crotalinae (organism)
Family cyclarhidae	Family Vireonidae (organism)
Family diomedeidae	Family Procellariidae (organism)
Family disruption NOS	Family disruption
Family disruption NOS	Family disruption
Family drepanididae	Subfamily Drepanidinae (organism)
Family dromadidae	Family Glareolidae (organism)
Family haematopodidae	Family Charadriidae (organism)
Family hippocastanaceae poisoning	Sapindaceae poisoning (disorder)
Family history of diabetes mellitus with complication	Family history of diabetes mellitus (situation)
Family history of malignant neoplasm of male breast	Family history of malignant neoplasm of breast (situation)
Family history of mental handicap	Family history of intellectual disability
Family history of mental retardation	Family history of intellectual disability
Family history of physical handicap	Family history of disability
Family history: Age at death	Age of family member at death (observable entity)
Family history: Blood disorder NOS	FH: Blood disorder
Family history: Brother NOS	FH: Brother
Family history: CVS disease NOS	FH: Cardiovascular disease
Family history: Congenital anomaly NOS	Family history of congenital disease (situation)
Family history: Daughter NOS	Family history with explicit context pertaining to daughter (situation)
Family history: Drug dependency	Family history of substance dependency
Family history: Ear disorder NOS	FH: Ear disorder
Family history: Endocrine disorder NOS	Family history of endocrine disorders (situation)
Family history: Eye disorder NOS	FH: Eye disorder
Family history: Father NOS	Family history with explicit context pertaining to father (situation)
Family history: Gastrointestinal disorder NOS	FH: Gastrointestinal disease
Family history: Infectious disease NOS	Family history of infectious disease (situation)
Family history: Mental disorder NOS	Family history of mental disorder
Family history: Mental handicap	Family history of intellectual disability
Family history: Metabolic disorder NOS	Family history of metabolic disorder
Family history: Mother NOS	Family history with explicit context pertaining to mother (situation)
Family history: Musculo-skeletal disorder NOS	FH: Musculoskeletal disease
Family history: NOS	Family history with explicit context (situation)
Family history: Relative NOS	Family history with explicit context (situation)
Family history: Relative OS	Family history with explicit context (situation)
Family history: Respiratory disease NOS	FH: Respiratory disease
Family history: Scleroderma	Family history of scleroderma
Family history: Sister NOS	Family history with explicit context pertaining to sister (situation)
Family history: Skin disease NOS	FH: Skin disease
Family history: Son NOS	Family history with explicit context pertaining to son (situation)
Family history: neoplasm - NOS	Family history of neoplasm
Family history: neoplasm - other intrathoracic organ	Family history of neoplasm
Family history: neoplasm - other lymphoid/hematopoietic	Family history of neoplasm
Family hyposittidae	Family Vangidae (organism)
Family loriidae	Family Psittacidae (organism)

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001156010	REPLACED BY association reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001157018	REPLACED BY association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)