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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Cysts (D003560)
Parent Node: Eyelid Diseases (D005141)
..Starting node ..Chalazion (D017043)
Child Nodes:
Sister Nodes:
..Barber Say syndrome (C537908)
..Blepharitis (D001762) 1
..Blepharochalasis, Superior (C566223)
..Blepharophimosis (D016569) 17
..Blepharoptosis (D001763) 24
..Blepharospasm (D001764) 2
..Chalazion (D017043)
..Cryptophthalmos, Unilateral or Bilateral, Isolated (C565138)
..Curly hair-ankyloblepharon-nail dysplasia syndrome (C538074)
..Eccrine Syringofibroadenomatosis with Eyelid Abnormalities (C566347)
..Ectropion (D004483) 2
..Entropion (D004774)
..Epiblepharon of Upper Lid (C565051)
..Eyelid Neoplasms (D005142) 2
..Hordeolum (D006726)
..Hyperpigmentation of Eyelids (C562400)
..Trichiasis (D058457)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1997
Name:	Chalazion
Definition:	A non-neoplastic cyst of the MEIBOMIAN GLANDS of the eyelid.
Alternative IDs:
ParentIDs:	MESH:D003560\|MESH:D005141
TreeNumbers:	C04.182.197 \|C11.338.300
Synonyms:	Chalazia \|Cyst, Meibomian \|Meibomian Cyst
Slim Mappings:	Cancer\|Eye disease
Reference:	MedGen: D017043 MeSH: D017043 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants