Experimental Factor Ontology
101 terms(s) returned
| Term Type: | Record: 1 to 50 of 101 Records | Page: 1 of 3, First Previous Next Last | Show Records Per Page |
- KAT6B-related multiple congenital anomalies syndrome
- KBG syndrome
- KCNH1 associated disorder
- KCNV2-related retinopathy
- KID syndrome
- KIF1A related neurological disorder
- KIF5A-related neurological disorder
- KIF7-related ciliopathy
- KINSSHIP syndrome
- KIZ-related retinopathy
- KLHL9-related early-onset distal myopathy
- Kabuki syndrome
- Kabuki syndrome 1
- Kabuki syndrome 2
- Kahrizi syndrome
- Kallmann syndrome
- Kallmann syndrome-heart disease syndrome
- Kandori fleck retina
- Kaposi sarcoma, susceptibility to
- Kapur-Toriello syndrome
- Karayol-Borroto-Haghshenas neurodevelopmental syndrome
- Kariminejad neurodevelopmental syndrome
- Karsch-Neugebauer syndrome
- Kaya-Barakat-Masson syndrome
- Kearns-Sayre syndrome
- Keipert syndrome
- Kennedy disease
- Kenny-Caffey syndrome
- Keppen-Lubinsky syndrome
- Keratocystic odontogenic tumor
- Keutel syndrome
- Khan-Khan-Katsanis syndrome
- Kilquist syndrome
- Kindler syndrome
- King-Denborough syndrome
- Klebsiella infectious disease
- Klebsiella pneumonia
- Kleefstra syndrome
- Kleefstra syndrome 1
- Kleefstra syndrome 2
- Kleefstra syndrome due to 9q34 microdeletion
- Kleefstra syndrome due to a point mutation
- 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
- Kniest dysplasia
- Knobloch syndrome
- Knobloch syndrome 1
