Experimental Factor Ontology
1020 terms(s) returned
Term Type: Class | Record: 51 to 100 of 1020 Records | Page: 2 of 21, First Previous Next Last | Show Records Per Page |
- Patterson-Stevenson-Fontaine syndrome
- Pearson syndrome
- Pediculus humanus corporis infestation
- Pelger-Huet-like anomaly and episodic fever with abdominal pain
- Pelizaeus-Merzbacher disease in female carriers
- Pelizaeus-Merzbacher disease, classic form
- Pelizaeus-Merzbacher disease, connatal form
- Pelizaeus-Merzbacher disease, transitional form
- Pelizaeus-Merzbacher-like disease
- Pelizeaus-Merzbacher spectrum disorder
- Pendred syndrome
- Perlman syndrome
- Perrault syndrome
- Perrault syndrome 1
- Perrault syndrome 2
- Perrault syndrome 4
- Perrault syndrome 5
- Perry syndrome
- Peters anomaly
- Peters anomaly-cataract syndrome
- Peters plus syndrome
- Peutz-Jeghers syndrome
- Peyronie disease
- Pfeiffer syndrome
- Pfeiffer syndrome type 1
- Pfeiffer syndrome type 2
- Pfeiffer syndrome type 3
- Pfeiffer-Palm-Teller syndrome
- Phelan-McDermid syndrome
- Pierpont syndrome
- Pierre Robin syndrome-faciodigital anomaly syndrome
- Pierson syndrome
- Pilotto syndrome
- Pitt-Hopkins syndrome
- Pitt-Hopkins-like syndrome
- Pitt-Hopkins-like syndrome 2
- Poirier-Bienvenu neurodevelopmental syndrome
- Poland syndrome
- Polymerase proofreading-related adenomatous polyposis
- Potocki-Lupski syndrome
- Potocki-Shaffer syndrome
- PrP systemic amyloidosis
- Prader-Willi syndrome
- Prader-Willi syndrome due to imprinting mutation
- Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
- Prader-Willi syndrome due to paternal 15q11q13 deletion
- Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
- Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
- Prader-Willi syndrome due to translocation
- Prader-Willi-like syndrome