Mondo Disease Ontology
2494 terms(s) returned
Term Type: | Record: 1901 to 1950 of 2494 Records | Page: 39 of 50, First Previous Next Last | Show Records Per Page |
- hydroxylapatite
- hydroxymethylpyridine
- hydroxyphenylalanine
- hydroxyprolinemia
- hydroxypyridine
- hymen, imperforate
- hymen, imperforate, non-human animal
- hymenolepiasis
- hyobranchial muscle
- hyoglossus muscle
- hyoid apparatus
- hyoid arch skeleton
- hyoid bone
- hyoid neural crest
- hyper-IgE recurrent infection syndrome 1, autosomal dominant
- hyper-IgE recurrent infection syndrome 3, autosomal recessive
- hyper-IgE recurrent infection syndrome 4, autosomal recessive
- hyper-IgE recurrent infection syndrome 4A, autosomal dominant
- hyper-IgE recurrent infection syndrome 5, autosomal recessive
- hyper-IgE syndrome
- hyper-IgE syndrome 6, autosomal dominant, with recurrent infections
- hyper-IgM syndrome
- hyper-IgM syndrome type 1
- hyper-IgM syndrome type 2
- hyper-IgM syndrome type 3
- hyper-IgM syndrome type 4
- hyper-IgM syndrome type 5
- hyper-beta-alaninemia
- hyperactivity
- hyperacusis
- hyperadrenocorticism, dog
- hyperadrenocorticism, domestic cat
- hyperadrenocorticism, domestic ferret
- hyperadrenocorticism, golden hamster
- hyperadrenocorticism, horse
- hyperadrenocorticism, non-human animal
- hyperaldosteronism
- hyperaldosteronism, domestic cat
- hyperaldosteronism, familial, type IV
- hyperaldosteronism, non-human animal
- hyperalphalipoproteinemia
- hyperammonemia due to N-acetylglutamate synthase deficiency
- hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
- hyperamylasemia
- hyperbilirubinemia
- hyperbilirubinemia, conjugated, type 3
- hyperbilirubinemia, non-human animal
- hyperbilirubinemia, shunt, primary
- hyperbiliverdinemia
- hypercalcemia disease