Experimental Factor Ontology
1401 terms(s) returned
Term Type: Class | Record: 1101 to 1150 of 1401 Records | Page: 23 of 29, First Previous Next Last | Show Records Per Page |
- congenital hemangioma
- congenital hematological disorder
- congenital hereditary endothelial dystrophy of cornea
- congenital hereditary endothelial dystrophy type I
- congenital hereditary facial paralysis-variable hearing loss syndrome
- congenital herpes simplex virus infection
- congenital herpes virus infection
- congenital high-molecular-weight kininogen deficiency
- congenital hydrocephalus
- congenital hydronephrosis
- congenital hypogonadotropic hypogonadism
- congenital hypothalamic hamartoma syndrome
- congenital hypothyroidism
- congenital hypotonia, epilepsy, developmental delay, and digital anomalies
- congenital hypotrichosis with juvenile macular dystrophy
- congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome
- congenital ichthyosis-microcephalus-tetraplegia syndrome
- congenital insensitivity to pain with hyperhidrosis
- congenital insensitivity to pain-hypohidrosis syndrome
- congenital isolated hyperinsulinism
- congenital knee dislocation
- congenital lactase deficiency
- congenital lactic acidosis, Saguenay-Lac-Saint-Jean type
- congenital laryngeal web
- congenital laryngomalacia
- congenital lethal erythroderma
- congenital limb malformation
- congenital lipoid adrenal hyperplasia due to STAR deficency
- congenital lobar emphysema
- congenital macroglossia
- congenital malabsorptive diarrhea 4
- congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization
- congenital merosin-deficient muscular dystrophy 1A
- congenital mesoblastic nephroma
- congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
- congenital microcoria
- congenital mitral stenosis
- congenital mitral valve insufficiency
- congenital mitral valve insufficiency and/or stenosis
- congenital multicore myopathy with external ophthalmoplegia
- congenital muscular dystrophy
- congenital muscular dystrophy 1B
- congenital muscular dystrophy caused by variation in POMGNT2
- congenital muscular dystrophy due to LMNA mutation
- congenital muscular dystrophy due to integrin alpha-7 deficiency
- congenital muscular dystrophy with hyperlaxity
- congenital muscular dystrophy with intellectual disability
- congenital muscular dystrophy with intellectual disability and severe epilepsy
- congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
- congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome