Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:130720	LATERAL MENINGOCELE SYNDROME; LMNS	—	—	—
OMIM	OMIM:130900	AMELOGENESIS IMPERFECTA, TYPE IIIA; AI3A	—	—	—
OMIM	OMIM:130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD	—	—	—
OMIM	OMIM:131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I; MEN1	—	—	—
OMIM	OMIM:131200	ENDOMETRIOSIS, SUSCEPTIBILITY TO, 1	—	—	—
OMIM	OMIM:131240	ENDOTHELIN 1; EDN1	—	—	—
OMIM	OMIM:131300	CAMURATI-ENGELMANN DISEASE; CAEND	—	—	—
OMIM	OMIM:131375	ENOLASE, SPERM SPECIFIC; ENO4	—	—	—
OMIM	OMIM:131400	EOSINOPHILIA, FAMILIAL	—	—	—
OMIM	OMIM:131430	EOSINOPHILOPENIA	—	—	—
OMIM	OMIM:131440	MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA	—	—	—
OMIM	OMIM:131445	MOVED TO 137800	—	—	—
OMIM	OMIM:131450	EPIBLEPHARON OF LOWER LID	—	—	—
OMIM	OMIM:131460	EPIBLEPHARON OF UPPER LID	—	—	—
OMIM	OMIM:131500	EPICANTHUS	—	—	—
OMIM	OMIM:131600	EPIDERMOID CYSTS	—	—	—
OMIM	OMIM:131705	TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN; TBDN	—	—	—
OMIM	OMIM:131750	EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT; DDEB	—	—	—
OMIM	OMIM:131760	EPIDERMOLYSIS BULLOSA SIMPLEX, DOWLING-MEARA TYPE; EBSDM	—	—	—
OMIM	OMIM:131800	EPIDERMOLYSIS BULLOSA SIMPLEX, LOCALIZED	—	—	—
OMIM	OMIM:131850	EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL	—	—	—
OMIM	OMIM:131880	EPIDERMOLYSIS BULLOSA WITH DEFICIENCY OF GALACTOSYLHYDROXYLYSYL GLUCOSYLTRANSFERASE	—	—	—
OMIM	OMIM:131900	EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED	—	—	—
OMIM	OMIM:131950	EPIDERMOLYSIS BULLOSA SIMPLEX, OGNA TYPE; EBSOG	—	—	—
OMIM	OMIM:131960	EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION; EBSMP	—	—	—