82859000: Macula lutea structure (body structure)

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Macula lutea structure	Is a	Zone of retina	false	Inferred relationship	Some
Macula lutea structure	Is a	repère anatomique	false	Inferred relationship	Some
Macula lutea structure	Is a	caractéristique anatomique	false	Inferred relationship	Some
Macula lutea structure	partie de	Entire retina	false	Inferred relationship	Some
Macula lutea structure	Laterality	Side (qualifier value)	true	Inferred relationship	Some
Macula lutea structure	partie de	Entire posterior pole of eye (body structure)	false	Additional relationship	Some
Macula lutea structure	Is a	Structure of optic portion of retina	true	Inferred relationship	Some
Macula lutea structure	Is a	Structure of posterior pole of retina (body structure)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Full thickness hole of macula lutea (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Injection of drug or medicament into macula (procedure)	Procedure site - Indirect (attribute)	False	Macula lutea structure	Inferred relationship	Some	1
Injection of drug or medicament into macula (procedure)	Procedure site - Indirect (attribute)	True	Macula lutea structure	Inferred relationship	Some	1
à l'examen : maculopathie diabétique de l'œil droit	Finding site	False	Macula lutea structure	Inferred relationship	Some	1
à l'examen : œdème maculaire de l'œil gauche cliniquement significatif	Finding site	False	Macula lutea structure	Inferred relationship	Some	1
Mixed maculopathy due to diabetes mellitus	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Focal exudative maculopathy due to diabetes mellitus	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Exudative maculopathy due to type 1 diabetes mellitus (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
à l'examen : maculopathie diabétique de l'œil gauche	Finding site	False	Macula lutea structure	Inferred relationship	Some	1
Disorder of macula due to diabetes mellitus	Finding site	False	Macula lutea structure	Inferred relationship	Some	1
Advanced maculopathy due to diabetes mellitus (disorder)	Finding site	False	Macula lutea structure	Inferred relationship	Some	1
Diffuse exudative maculopathy due to diabetes mellitus (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Ischemic maculopathy due to diabetes mellitus (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Exudative maculopathy due to type 2 diabetes mellitus (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Degeneration of macula due to cyst or hole	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Macular focal choroiditis	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Repair of hole of macula lutea	Procedure site - Direct (attribute)	True	Macula lutea structure	Inferred relationship	Some	1
Congenital anomaly of macula	Finding site	False	Macula lutea structure	Inferred relationship	Some	2
Congenital anomaly of macula	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Macular edema and retinopathy due to type 2 diabetes mellitus (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Congenital macular changes	Finding site	False	Macula lutea structure	Inferred relationship	Some	3
Mixed maculopathy due to diabetes mellitus	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Fundus flavimaculatus	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Stargardt's disease	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
The following must be present on at least one OCT (Optical coherence tomography) scan image: (i) Partial vitreous detachment as indicated by elevation of cortical vitreous above the retinal surface in the perifoveal area (ii) Persistent vitreous attachment.	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Persistent placoid maculopathy is characterized by white plaque-like lesions involving the macula but sparing the peripapillary areas of both eyes. It has been described in five patients. In contrast to patients with macular serpiginous choroiditis presenting with similar lesions, the five patients reported so far with persistent placoid maculopathy had good visual acuity until the onset of choroidal neovascularization (CNV) or pigmentary mottling. The macular lesions fade after several months or years, but the vascular anomalies persist leading to a loss of central vision.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Benign concentric annular macular dystrophy (BCAMD) is a progressive autosomal dominant macular dystrophy characterized by parafoveal hypopigmentation followed by a retinitis pigmentosa-like phenotype (nyctalopia and peripheral vision loss) with a bull's eye configuration.	Finding site	False	Macula lutea structure	Inferred relationship	Some
A rare ectodermal dysplasia syndrome characterized by the association of ectodermal dysplasia (with hypotrichosis affecting scalp hair, eyebrows, and eyelashes, and partial anodontia), ectrodactyly, and macular dystrophy (appearing as a central geographic atrophy of the retinal pigment epithelium and choriocapillary layer of the macular area with coarse hyperpigmentations and sparing of the larger choroidal vessels). Variable additional limb defects (including absence deformities, polydactyly, syndactyly, or camptodactyly) have also been described, the hands often being more severely affected than the feet.	Finding site	False	Macula lutea structure	Inferred relationship	Some	5
A rare congenital malformation syndrome characterized by the combination of bilateral coloboma of macula with horizontal pendular nystagmus and severe visual loss, and brachydactyly type B. The hand and feet defects comprise of shortening of the middle and terminal phalanges of the second to fifth digits, hypoplastic or absent nails (congenital anonychia), broad or bifid thumbs and halluces, syndactyly and flexion deformities of the joints of some digits.	Finding site	False	Macula lutea structure	Inferred relationship	Some	4
Structure of macula lutea of right eye (body structure)	Is a	True	Macula lutea structure	Inferred relationship	Some
Structure of macula lutea of left eye (body structure)	Is a	True	Macula lutea structure	Inferred relationship	Some
Full thickness macular hole of left eye (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Full thickness macular hole of right eye (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Macular coloboma-cleft palate-hallux valgus syndrome is characterized by the association of bilateral macular coloboma, cleft palate, and hallux valgus. It has been described in a brother and sister. Pelvic, limb and digital anomalies were also reported. Transmission is autosomal recessive.	Finding site	False	Macula lutea structure	Inferred relationship	Some	6
Hypotrichosis with juvenile macular degeneration (HJMD) is a very rare syndrome characterized by sparse and short hair from birth followed by progressive macular degeneration leading to blindness.	Finding site	False	Macula lutea structure	Inferred relationship	Some	5
A rare and severe inborn metabolic disease characterized clinically by the association of severe-to-profound neurodevelopmental impairment, severe visual impairment, ante-postnatal growth impairment, severe scoliosis and, frequently, early-onset epilepsy.	Finding site	False	Macula lutea structure	Inferred relationship	Some	2
A rare congenital malformation syndrome characterized by the combination of bilateral coloboma of macula with horizontal pendular nystagmus and severe visual loss, and brachydactyly type B. The hand and feet defects comprise of shortening of the middle and terminal phalanges of the second to fifth digits, hypoplastic or absent nails (congenital anonychia), broad or bifid thumbs and halluces, syndactyly and flexion deformities of the joints of some digits.	Finding site	False	Macula lutea structure	Inferred relationship	Some	1
Macular coloboma-cleft palate-hallux valgus syndrome is characterized by the association of bilateral macular coloboma, cleft palate, and hallux valgus. It has been described in a brother and sister. Pelvic, limb and digital anomalies were also reported. Transmission is autosomal recessive.	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Telangiectasia of macula lutea	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Traumatic macular hole	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Coloboma of macula is a rare, non-syndromic developmental defect of the eye characterized by well-circumscribed, oval or rounded, usually unilateral, atrophic lesions of varying size presenting rudimentary or absent retina, choroid and sclera located at the macula leading to decreased vision and, on occasion, other symptoms (e.g. strabismus). It is usually isolated, but may also be associated with Down syndrome, skeletal or renal disorders.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Best vitelliform macular dystrophy (BVMD) is a genetic macular dystrophy characterized by loss of central visual acuity, metamorphopsia and a decrease in the Arden ratio secondary to an egg yolk-like lesion located in the foveal or parafoveal region.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Toxic maculopathy caused by antimalarial agent	Finding site	False	Macula lutea structure	Inferred relationship	Some	1
A rare, genetic, macular dystrophy characterized by blurred vision, metamorphopsia and mild visual impairment secondary to a slightly elevated, yellow, egg yolk-like lesion located in the foveal or parafoveal region.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
dystrophie vitelliforme	Finding site	False	Macula lutea structure	Inferred relationship	Some	1
Clinically significant macular edema due to diabetes mellitus	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Advanced maculopathy due to diabetes mellitus (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Macular edema due to type 1 diabetes mellitus	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Macular edema due to type 2 diabetes mellitus	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Disorder of macula due to diabetes mellitus	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Retinal macular dystrophy type 2 is a rare, genetic macular dystrophy disorder characterized by slowly progressive bull eye maculopathy associated, in most cases, with mild decrease in visual acuity and central scotomata. Usually, only the central retina is involved, however some cases of more widespread rod and cone anomalies have been reported. Rare additional features include empty sella turcica, impaired olfaction, renal infections, hematuria and recurrent miscarriages.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Benign concentric annular macular dystrophy (BCAMD) is a progressive autosomal dominant macular dystrophy characterized by parafoveal hypopigmentation followed by a retinitis pigmentosa-like phenotype (nyctalopia and peripheral vision loss) with a bull's eye configuration.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Bull's eye macular dystrophy	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
North Carolina macular dystrophy	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Dominant drusen	Finding site	False	Macula lutea structure	Inferred relationship	Some	1
Hereditary macular dystrophy	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Occult macular dystrophy is a rare, genetic retinal dystrophy disease characterized by bilateral progressive decline of visual acuity, due to retinal dysfunction confined only to the macula, associated with normal fundus and fluorescein angiograms and severly attenuated focal macular and multifocal electroretinograms.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
A rare progressive autosomal dominant macular dystrophy, presenting between the third and sixth decades of life, with characteristics of retinal atrophy and retinal detachment leading to loss of central vision, then peripheral vision, and eventually blindness.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
A rare and severe inborn metabolic disease characterized clinically by the association of severe-to-profound neurodevelopmental impairment, severe visual impairment, ante-postnatal growth impairment, severe scoliosis and, frequently, early-onset epilepsy.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
A rare ectodermal dysplasia syndrome characterized by the association of ectodermal dysplasia (with hypotrichosis affecting scalp hair, eyebrows, and eyelashes, and partial anodontia), ectrodactyly, and macular dystrophy (appearing as a central geographic atrophy of the retinal pigment epithelium and choriocapillary layer of the macular area with coarse hyperpigmentations and sparing of the larger choroidal vessels). Variable additional limb defects (including absence deformities, polydactyly, syndactyly, or camptodactyly) have also been described, the hands often being more severely affected than the feet.	Finding site	True	Macula lutea structure	Inferred relationship	Some	3
Hypotrichosis with juvenile macular degeneration (HJMD) is a very rare syndrome characterized by sparse and short hair from birth followed by progressive macular degeneration leading to blindness.	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
A rare congenital malformation syndrome characterized by the combination of bilateral coloboma of macula with horizontal pendular nystagmus and severe visual loss, and brachydactyly type B. The hand and feet defects comprise of shortening of the middle and terminal phalanges of the second to fifth digits, hypoplastic or absent nails (congenital anonychia), broad or bifid thumbs and halluces, syndactyly and flexion deformities of the joints of some digits.	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Idiopathic macular telangiectasia type 1 is a rare, acquired, eye disease characterized by unilateral (rarely bilateral) abnormally dilated and tortuous capillaries around the fovea, associated with multiple arteriolar and venular aneurysms, lipid depositions, and intra-retinal cystoid degeneration. It leads to vision loss due to macular edema with hard exudates.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Idiopathic macular telangiectasia type 3 is a rare, acquired, eye disease characterized by progressive visual loss, due to bilateral juxtafoveolar capillary occlusions, capillary telangiectasia, and minimal exudation. It is associated with systemic or cerebral vascular occlusive disease.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Toxic maculopathy	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Macular retinoschisis	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Macular and peripheral retinoschisis	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Macular and peripheral retinoschisis	Finding site	True	Macula lutea structure	Inferred relationship	Some	4
Macular vitelliform deposits	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
dégénérescence de la macula et du pôle postérieur	Finding site	False	Macula lutea structure	Inferred relationship	Some	2
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Early age related macular degeneration	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Intermediate age related macular degeneration (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Small drusen of the macula	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Atrophy of macula lutea	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Retinal angiomatous proliferation	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Idiopathic macular telangiectasia type 2 (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Idiopathic juxtafoveal telangiectasia (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Macular exudate (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Leber idiopathic stellate neuroretinitis	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Cystoid macular edema due to diabetes mellitus (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Persistent macular oedema due to diabetes mellitus	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Centrally involved macular edema due to diabetes mellitus (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Non centrally involved macular oedema due to diabetes mellitus	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Traumatic macular hole	Finding site	True	Macula lutea structure	Inferred relationship	Some	3
Vitreomacular adhesion (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
Macular subretinal fibrosis	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
A lysosomal storage disease with characteristics of coarse facial features, macular cherry red spot, and dysostosis multiplex. Clinical presentation can be heterogeneous ranging from a severe, early-onset, rapidly progressive infantile form to late onset, slowly progressive juvenile/adult form.	Finding site	True	Macula lutea structure	Inferred relationship	Some	4
Diffuse exudative maculopathy due to diabetes mellitus (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	2
A rare, genetic retinal disease characterized by the characteristic dried-out soil fundus pattern due to diffuse deep white lines in the macula, to the level of the retinal pigment epithelium, which is slightly elevated and rippled. Macular exudation may be associated, and Bruch's membrane may be affected too. Occasionally, peripheral nummular pigmentary changes may be observed, associated with blindness. The lesions enlarge with time, with a preferential macular extension and confluence. Complications may include polypoidal choroidal vasculopathy, choroidal neovascularization or atrophic fibrous macular scarring that can lead to reduced visual acuity over time.	Finding site	False	Macula lutea structure	Inferred relationship	Some	1
A rare genetic eye disease characterized by optic disc anomalies (bilateral colobomatous optic discs, retinal vessels arising from the peripheral optic disc) and macular atrophy. Peripapillary chorioretinal atrophy and chorioretinal and iris coloboma have also been described. Patients present with horizontal nystagmus and poor visual acuity.	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Advanced age related macular degeneration (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Advanced exudative age related macular degeneration (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Cystoid macular oedema following cataract surgery	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Paracentral acute middle maculopathy (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Macular ischemia due to central retinal vein occlusion (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	3
Macular focal retinitis	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Macular focal choroiditis of bilateral eyes (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	5
Paramacular focal retinitis AND retinochoroiditis	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Macular hole due to degenerative high myopia	Finding site	True	Macula lutea structure	Inferred relationship	Some	1
Ischemic disorder of macula lutea due to occlusion of retinal branch vein (disorder)	Finding site	True	Macula lutea structure	Inferred relationship	Some	1

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Id	Description	Lang	Type	Status	Case?	Module
137445014	Macula lutea	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
505299014	Macula lutea structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
824369016	Macula lutea structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core