Mondo Disease Ontology
5650 terms(s) returned
| Term Type: | Record: 1101 to 1150 of 5650 Records | Page: 23 of 113, First Previous Next Last | Show Records Per Page |
- 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
- Prata-Liberal-Goncalves syndrome
- Pre-capillary pulmonary hypertension
- Preaxial foot polydactyly
- Preaxial hand polydactyly
- Preaxial polydactyly
- Preaxial polydactyly of toes
- Preaxial polydactyly of toes, bilateral
- Preaxial polydactyly of toes, unilateral
- Precocious costochondral ossification
- Precocious puberty
- Precocious puberty in females
- Preeyasombat-Varavithya syndrome
- Pregnancy history
- Premature birth
- Premature chromatid separation
- Premature closure of fontanelles
- Premature ejaculation
- Prenatal death
- Prenatal movement abnormality
- Prepapillary vascular loops
- Preplasmiviricota
- Prepoliviricotina
- Prescottella
- Prescottella equi
- Presence of a Hormonal Syndrome
- Priapism
- Prieto syndrome
- Primary adrenal insufficiency
- Primary hypothyroidism
- Primate T-lymphotropic virus 1
- Primate T-lymphotropic virus 2
- Primate lentivirus group
- Primates
- Primrose syndrome
- Prinzmetal angina
- Proboscidea <placentals>
- Procedure_Has_Target_Anatomy
- Procyon
- Procyon lotor
- Procyonidae
- Progesterone Receptor Negative
- Progesterone Receptor Positive
- Progesterone Receptor Status
- Progressive
