Mondo Disease Ontology
1479 terms(s) returned
| Term Type: | Record: 1 to 50 of 1479 Records | Page: 1 of 30, First Previous Next Last | Show Records Per Page |
- H syndrome
- HAND1 related congenital heart defect
- HAND2 related congenital heart defect
- HBA1-related alpha thalassemia spectrum
- HBA1; HBA2-related digenic alpha thalassemia spectrum
- HBA2-related alpha thalassemia spectrum
- HEC syndrome
- HELIOS deficiency
- HELIX syndrome
- HELLP syndrome
- HER2 positive breast carcinoma
- HGSNAT-related retinopathy
- HHV-6 encephalitis
- HHV-7 infectious disease
- HIV enteropathy
- HIV infectious disease
- HIV wasting syndrome
- HIV-associated cancer
- HIV-associated nephropathy
- HNRNPC-related neurodevelopmental disorder
- HSD10 disease, atypical type
- HSD10 disease, infantile type
- HSD10 disease, neonatal type
- HSD10 mitochondrial disease
- HTLV-2 infection
- HTRA1-related autosomal dominant cerebral small vessel disease
- Haddad syndrome
- Hailey-Hailey disease
- Haim-Munk syndrome
- Hall-Riggs syndrome
- Hallermann-Streiff syndrome
- Halothane hepatitis
- Hantavirus hemorrhagic fever with renal syndrome, Dobrava-Belgrade virus type
- Hantavirus hemorrhagic fever with renal syndrome, Puumala virus type
- Hantavirus hemorrhagic fever with renal syndrome, Seoul virus type
- Hao-Fountain syndrome
- Hao-Fountain syndrome due to 16p13.2 microdeletion
- Hao-Fountain syndrome due to USP7 mutation
- Happle-Tinschert syndrome
- Harel-Yoon syndrome
- Harrod syndrome
- Hartnup disease
- Hartsfield-Bixler-Demyer syndrome
- Hashimoto thyroiditis
- Hashimoto-Pritzker syndrome
- Hb Bart's hydrops fetalis
- Heberden's node
- Heiner syndrome
- Heinz body anemia
- Helicobacter pylori infection, susceptibility to
