Mondo Disease Ontology
5650 terms(s) returned
| Term Type: | Record: 501 to 550 of 5650 Records | Page: 11 of 113, First Previous Next Last | Show Records Per Page |
- PROM1-related dominant retinopathy
- PROM1-related recessive retinopathy
- PROM1-related retinopathy
- PROP1
- PRORP
- PROS1
- PROZ
- PRPF19
- PRPF19-related neurodevelopmental disorder
- PRPF3
- PRPF31
- PRPF31-related retinopathy
- PRPF4
- PRPF6
- PRPF8
- PRPF8-related retinopathy
- PRPH
- PRPH2
- PRPH2-related retinopathy
- PRPS1
- PRPS1 deficiency disorder
- PRR12
- PRRT2
- PRRT2-associated paroxysmal movement disorder
- PRRX1
- PRSS1
- PRSS12
- PRSS2
- PRSS56
- PRUNE1
- PRX
- PRY
- PRY2
- PSAP
- PSAP-related sphingolipidosis
- PSAT deficiency
- PSAT1
- PSEN1
- PSEN1
- PSEN1
- PSEN1
- PSEN2
- PSENEN
- PSKH1
- PSMA6
- PSMB10
- PSMB8
- PSMB9
- PSMC3IP
- PSMD12
