Weill-Marchesani syndrome 3 - Ontology Browser

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Weill-Marchesani syndrome 3 (EFO:MONDO:0013899)
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Parent Terms

Term With Siblings

Child Terms

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma +

Weill-Marchesani 4 syndrome, recessive

Weill-Marchesani syndrome 2, dominant

Weill-Marchesani syndrome 3

Any Weill-Marchesani syndrome in which the cause of the disease is a mutation in the LTBP2 gene.

Synonyms
Exact Synonyms:	LTBP2 Weill-Marchesani syndrome ; Weill-Marchesani syndrome 3, recessive ; Weill-Marchesani syndrome caused by mutation in LTBP2 ; Weill-Marchesani syndrome type 3 ; http://identifiers.org/medgen/766699 ; http://linkedlifedata.com/resource/umls/id/C3553785 ; https://omim.org/entry/614819
Related Synonyms:	WMS3
Alternate IDs:	MONDO:0013899
Xrefs:	GARD:15844 ; MEDGEN:766699 ; MIM:614819 ; UMLS:C3553785
Definition Sources:	MONDO:patterns/disease_series_by_gene

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