Mondo Disease Ontology
2169 terms(s) returned
| Term Type: | Record: 2051 to 2100 of 2169 Records | Page: 42 of 44, First Previous Next Last | Show Records Per Page |
- isolated congenital anosmia
- isolated congenital auditory ossicle malformation
- isolated congenital breast hypoplasia/aplasia
- isolated congenital cholesteatoma of the middle ear
- isolated congenital digital clubbing
- isolated congenital ectropion
- isolated congenital entropion
- isolated congenital femoral bifurcation
- isolated congenital growth hormone deficiency
- isolated congenital hepatic fibrosis
- isolated congenital hypoglossia
- isolated congenital hypoglossia/aglossia
- isolated congenital hypogonadotropic hypogonadism
- isolated congenital megalocornea
- isolated congenital microcephaly
- isolated congenital nasal pyriform aperture stenosis
- isolated congenital syngnathia
- isolated congenitally uncorrected transposition of the great arteries
- isolated craniosynostosis
- isolated cryptophthalmia
- isolated delta-storage pool disease
- isolated duodenal duplication
- isolated dystonia
- isolated ectopia lentis
- isolated encephalocele
- isolated exencephaly
- isolated facial myokymia
- isolated familial wooly hair disorder
- isolated female hypospadias
- isolated filum lipoma
- isolated focal cortical dysplasia
- isolated focal cortical dysplasia type I
- isolated focal cortical dysplasia type II
- isolated focal cortical dysplasia type IIa
- isolated focal cortical dysplasia type IIb
- isolated focal cortical dysplasia type Ia
- isolated focal cortical dysplasia type Ib
- isolated focal cortical dysplasia type Ic
- isolated focal non-epidermolytic palmoplantar keratoderma
- isolated foveal hypoplasia
- isolated glycerol kinase deficiency
- isolated growth hormone deficiency type IA
- isolated growth hormone deficiency type IB
- isolated growth hormone deficiency type II
- isolated growth hormone deficiency type III
- isolated growth hormone deficiency, type 4
- isolated growth hormone deficiency, type 5
- isolated hemihyperplasia
- isolated hereditary congenital facial paralysis
- isolated hyperchlorhidrosis
