Experimental Factor Ontology
11113 terms(s) returned
| Term Type: | Record: 2751 to 2800 of 11113 Records | Page: 56 of 223, First Previous Next Last | Show Records Per Page |
- obsolete_Pfeiffer syndrome
- obsolete_Pfeiffer syndrome type 1
- obsolete_Pfeiffer syndrome type 2
- obsolete_Pfeiffer syndrome type 3
- obsolete_Pfeiffer-Palm-Teller syndrome
- obsolete_Pharyngeal Adenoid Cystic Carcinoma
- obsolete_Phlebitis
- obsolete_Phlebotomus fever
- obsolete_Phosphaturic Mesenchymal Tumor
- obsolete_Phosphoenolpyruvate carboxykinase 1 deficiency
- obsolete_Phosphoenolpyruvate carboxykinase 2 deficiency
- obsolete_Pick disease
- obsolete_Picornaviridae infectious disease
- obsolete_Pierson syndrome
- obsolete_Pilomatrixoma
- obsolete_Pilotto syndrome
- obsolete_Pima Indian
- obsolete_Pineal Parenchymal Tumor of Intermediate Differentiation
- obsolete_Pineoblastoma
- obsolete_Pineocytoma
- obsolete_Pitt-Hopkins syndrome
- obsolete_Pitt-Hopkins-like syndrome
- obsolete_Pituicytoma
- obsolete_Pituitary Gland Adenoma
- obsolete_Placental Choriocarcinoma
- obsolete_Placental Hemangioma
- obsolete_Plantar Fibromatosis
- obsolete_Plasmodium falciparum malaria
- obsolete_Plasmodium vivax malaria
- obsolete_Pleural Biphasic Mesothelioma
- obsolete_Pleural Epithelioid Mesothelioma
- obsolete_Pleural Mesothelioma
- obsolete_Pleural Sarcomatoid Mesothelioma
- obsolete_Pleuropulmonary blastoma
- obsolete_Plexiform Ameloblastoma
- obsolete_Pneumocystis infectious disease
- obsolete_Pneumonia, Aspiration
- obsolete_Poland syndrome
- obsolete_Polyarteritis Nodosa
- obsolete_Polycystic Kidney Disease
- obsolete_Polyomavirus infectious disease
- obsolete_Poorly Differentiated Thyroid Gland Carcinoma
- obsolete_Popov-Chang syndrome
- obsolete_Postthrombotic Syndrome
- obsolete_Potocki-Shaffer syndrome
- obsolete_Prader-Willi syndrome
- obsolete_Prader-Willi syndrome due to imprinting mutation
- obsolete_Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
- obsolete_Prader-Willi syndrome due to paternal 15q11q13 deletion
- obsolete_Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
