Mondo Disease Ontology
192 terms(s) returned
| Term Type: | Record: 1 to 50 of 192 Records | Page: 1 of 4, First Previous Next Last | Show Records Per Page |
- KAT6B-related multiple congenital anomalies syndrome
- KBG syndrome
- KCND2-related neurodevelopmental disorder with or without seizures
- KCNH1 associated disorder
- KDM3B-related intellectual disability-facial dysmorphism-short stature syndrome
- KID syndrome
- KIF1A related neurological disorder
- KIF7-related ciliopathy
- KINSSHIP syndrome
- KIZ-related retinopathy
- KLHL7-related Bohring-Opitz-like syndrome
- KLHL7-related cold-induced sweating-like syndrome
- KLHL9-related early-onset distal myopathy
- KSHV inflammatory cytokine syndrome
- Kabuki syndrome
- Kabuki syndrome 1
- Kabuki syndrome 2
- Kahrizi syndrome
- Kallmann syndrome
- Kallmann syndrome with spastic paraplegia
- Kallmann syndrome-heart disease syndrome
- Kandori fleck retina
- Kaplowitz-Bodurtha syndrome
- Kaposi sarcoma, susceptibility to
- Kaposi's sarcoma
- Kapur-Toriello syndrome
- Karsch-Neugebauer syndrome
- Kasabach-Merritt syndrome
- Kashani-Strom-Utley syndrome
- Kashin-Beck disease
- Kasznica-Carlson-Coppedge syndrome
- Katsantoni-Papadakou-Lagoyanni syndrome
- Kaya-Barakat-Masson syndrome
- Kearns-Sayre syndrome
- Keipert syndrome
- Kennedy disease
- Kenny-Caffey syndrome
- Keppen-Lubinsky syndrome
- Keratocystic odontogenic tumor
- Kerion celsi
- Keshan disease
- Keutel syndrome
- Khan-Khan-Katsanis syndrome
- Kienbock disease
- Kifafa seizure disorder
- Kikuchi-Fujimoto disease
- Kilquist syndrome
- Kimura disease
- Kindler syndrome
- King-Denborough syndrome
