Mondo Disease Ontology
5650 terms(s) returned
| Term Type: | Record: 301 to 350 of 5650 Records | Page: 7 of 113, First Previous Next Last | Show Records Per Page |
- PLG-related hereditary angioedema with normal C1inh
- PLIN1
- PLIN1-related familial partial lipodystrophy
- PLIN4
- PLK4
- PLN
- PLN
- PLOD1
- PLOD1
- PLOD2
- PLOD3
- PLP1
- PLP1
- PLP1
- PLP2
- PLPBP
- PLS1
- PLS3
- PLVAP
- PLXNA1
- PLXND1
- PMEL
- PMFBP1
- PMM2
- PMM2-congenital disorder of glycosylation
- PMP2
- PMP22
- PMP22-RAI1 contiguous gene duplication syndrome
- PMPCA
- PMPCB
- PMS1
- PMS2
- PMVK
- PNKD
- PNKP
- PNLDC1
- PNLIP
- PNP
- PNPLA1
- PNPLA1
- PNPLA2
- PNPLA6
- PNPLA6-related spastic paraplegia with or without ataxia
- PNPLA8
- PNPLA8
- PNPLA8
- PNPO
- PNPT1
- POC1A
- POC1B
