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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: Conjunctival Diseases (D003229)
..Starting node ..Pterygium (D011625)
Child Nodes:
........Fetal akinesia syndrome, X-linked (C537921)
........Haspeslagh Fryns Muelenaere syndrome (C535844)
........Powell Chandra Saal syndrome (C538357)
........Pterygium colli mental retardation digital anomalies (C535831)
........Pterygium Of Conjunctiva And Cornea (C566740)
........Rubinstein Taybi like syndrome (C535877)
........Thompson Baraitser syndrome (C536515)
Sister Nodes:
..Amyloidosis of Gingiva and Conjunctiva, with Mental Retardation (C565958)
..Conjunctival Neoplasms (D003230) 1
..Conjunctivitis (D003231) 12
..Laryngo onycho cutaneous syndrome (C537032)
..Pemphigoid, Benign Mucous Membrane (D010390)
..Pinguecula (D059407)
..Pterygium (D011625) 7
..Ring dermoid of cornea (C535684)
..Xerophthalmia (D014985)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9454
Name:	Pterygium
Definition:	An abnormal triangular fold of membrane in the interpalpebral fissure, extending from the conjunctiva to the cornea, being immovably united to the cornea at its apex, firmly attached to the sclera throughout its middle portion, and merged with the conjunctiva at its base. (Dorland, 27th ed)
Alternative IDs:
ParentIDs:	MESH:D003229
TreeNumbers:	C11.187.781
Synonyms:	Pterygiums
Slim Mappings:	Eye disease
Reference:	MedGen: D011625 MeSH: D011625 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants