Mondo Disease Ontology
5038 terms(s) returned
Term Type: Class | Record: 4151 to 4200 of 5038 Records | Page: 84 of 101, First Previous Next Last | Show Records Per Page |
- 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 human immunodeficiency virus
- congenital hydrocephalus
- congenital hydronephrosis
- congenital hypogonadotropic hypogonadism
- congenital hypoplasia of the mitral valve annulus
- congenital hypothalamic hamartoma syndrome
- congenital hypothyroidism
- congenital hypothyroidism due to maternal intake of antithyroid drugs
- congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies
- congenital hypothyroidism, chicken
- congenital hypothyroidism, dog
- congenital hypothyroidism, domestic cat
- congenital hypothyroidism, goat
- congenital hypothyroidism, horse
- congenital hypothyroidism, non-human animal
- congenital hypothyroidism, sheep
- congenital hypotonia, epilepsy, developmental delay, and digital anomalies
- congenital hypotrichosis milia
- congenital hypotrichosis with juvenile macular dystrophy
- congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome
- congenital ichthyosis-microcephalus-tetraplegia syndrome
- congenital infiltrating lipomatosis of the face
- congenital insensitivity to pain syndrome, Marsili type
- congenital insensitivity to pain with hyperhidrosis
- congenital insensitivity to pain with severe intellectual disability
- congenital insensitivity to pain-hypohidrosis syndrome
- congenital isolated adrenocorticotropic hormone deficiency
- congenital isolated hyperinsulinism
- congenital knee dislocation
- congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome
- congenital lactase deficiency
- congenital lactic acidosis, Saguenay-Lac-Saint-Jean type
- congenital laryngeal cyst
- congenital laryngeal palsy
- congenital laryngeal web
- congenital laryngomalacia
- congenital left-sided heart lesions
- congenital lethal erythroderma
- congenital limb malformation
- congenital lipoid adrenal hyperplasia due to STAR deficency
- congenital lobar emphysema
- congenital macroglossia
- congenital malabsorptive diarrhea 4
- congenital megacalycosis
- congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization