Mondo Disease Ontology
5568 terms(s) returned
| Term Type: | Record: 4501 to 4550 of 5568 Records | Page: 91 of 112, First Previous Next Last | Show Records Per Page |
- congenital disorder of glycosylation, type IIy
- congenital disorder of glycosylation, type IIz
- congenital disorder of glycosylation, type Ibb
- congenital disorder of glycosylation, type Iw, autosomal dominant
- congenital disorder of glycosylation, type i/IIx
- congenital disorder of glycosylation, type iit
- congenital dyserythropoietic anemia
- congenital dyserythropoietic anemia type 1
- congenital dyserythropoietic anemia type 2
- congenital dyserythropoietic anemia type 3
- congenital dyserythropoietic anemia type 4
- congenital dyserythropoietic anemia type type 1B
- congenital dyserythropoietic anemia with dyskeratosis and progressive alopecia, cattle
- congenital dyserythropoietic anemia with dyskeratosis and progressive alopecia, non-human animal
- congenital dyserythropoietic anemia, cattle
- congenital dyserythropoietic anemia, non-human animal
- congenital dyshormonogenic hypothyroidism with goiter, SLC5A5-related, dog
- congenital ectropion
- congenital ectropion uveae
- congenital elbow dislocation
- congenital elbow dislocation, bilateral
- congenital elbow dislocation, unilateral
- congenital emphysematous lung disease due to Filamin A loss-of-function variant
- congenital enterocyte heparan sulfate deficiency
- congenital enteropathy due to enteropeptidase deficiency
- congenital enterovirus infection
- congenital entropion
- congenital epulis
- congenital erosive and vesicular dermatosis
- congenital erythropoietic porphyria, cattle
- congenital erythropoietic porphyria, domestic cat
- congenital erythropoietic porphyria, non-human animal
- congenital erythropoietic porphyria, pig
- congenital erythropoietic porphyria, zebu cattle
- congenital esophageal diverticulum
- congenital esophageal stenosis
- congenital eye malformation, SIX6-related, dog
- congenital eyelid retraction
- congenital factor V deficiency
- congenital factor VII deficiency
- congenital factor X deficiency
- congenital factor XI deficiency
- congenital factor XII deficiency
- congenital factor XIII deficiency
- congenital fiber-type disproportion myopathy
- congenital fibrinogen deficiency
- congenital fibrosarcoma
- congenital fibrosis of extraocular muscles
- congenital fibrosis of extraocular muscles type 1
- congenital generalized hypercontractile muscle stiffness syndrome
