Mondo Disease Ontology
511 terms(s) returned
| Term Type: | Record: 251 to 300 of 511 Records | Page: 6 of 11, First Previous Next Last | Show Records Per Page |
- Kit-positive, Sca1-positive common lymphoid progenitor
- Kit-positive, integrin beta7-high basophil mast progenitor cell
- Kitrinoviricota
- Klebsiella
- Klebsiella granulomatis
- Klebsiella infectious disease
- Klebsiella pneumonia
- Klebsiella pneumoniae
- Klebsiella pneumoniae complex
- Klebsiella/Raoultella group
- Kleefstra syndrome
- Kleefstra syndrome 1
- Kleefstra syndrome 2
- Kleefstra syndrome due to 9q34 microdeletion
- Kleefstra syndrome due to a point mutation
- Kleine-Levin syndrome
- Klinefelter syndrome
- Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
- Klippel-Feil syndrome
- Klippel-Feil syndrome 1, autosomal dominant
- Klippel-Feil syndrome 2, autosomal recessive
- Klippel-Feil syndrome 3, autosomal dominant
- Kluver-Bucy syndrome
- Knee contracture
- Knee dislocation
- Knee flexion contracture
- Knee joint hypermobility
- Kniest dysplasia
- Kniest-like dysplasia with pursed lips and ectopia lentis
- Knobloch syndrome
- Knobloch syndrome 1
- Knobloch syndrome 2
- Kocher-debre-Semelaigne syndrome
- Kohlschutter-Tonz syndrome-like
- Kolmioviridae
- Kommerell diverticulum
- Koolen-de Vries syndrome
- Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome
- Koolen-de Vries syndrome due to a point mutation
- Koone-Rizzo-Elias syndrome
- Kostmann syndrome
- Kotzot-Richter syndrome
- Kousseff syndrome
- Kozlowski Brown Hardwick syndrome
- Kozlowski Ouvrier syndrome
- Kozlowski Rafinski Klicharska syndrome
- Kozlowski Warren Fisher syndrome
- Krabbe disease
- Krabbe disease due to saposin A deficiency
- Krabbe disease, Rhesus monkey
