Experimental Factor Ontology
1932 terms(s) returned
| Term Type: | Record: 351 to 400 of 1932 Records | Page: 8 of 39, First Previous Next Last | Show Records Per Page |
- Rare female infertility due to a congenital hypogonadotropic hypogonadism
- Rare female infertility due to adrenal disorder of genetic origin
- Rare female infertility due to an anomaly of ovarian function of genetic origin
- Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
- Rare genetic adrenal disease
- Rare genetic bone development disorder
- Rare genetic bone disease
- Rare genetic cardiac disease
- Rare genetic coagulation disorder
- Rare genetic deafness
- Rare genetic developmental defect during embryogenesis
- Rare genetic diabetes mellitus
- Rare genetic disease with myoclonus as a major feature
- Rare genetic disorder with obstructive azoospermia
- Rare genetic dystonia
- Rare genetic endocrine disease
- Rare genetic epilepsy
- Rare genetic eye disease
- Rare genetic female infertility
- Rare genetic gastroenterological disease
- Rare genetic headache
- Rare genetic hematologic disease
- Rare genetic hepatic disease
- Rare genetic hypothalamic or pituitary disease
- Rare genetic immune disease
- Rare genetic intellectual disability
- Rare genetic intellectual disability with developmental anomaly
- Rare genetic male infertility
- Rare genetic medullar disease
- Rare genetic movement disorder
- Rare genetic neurological disorder
- Rare genetic odontologic disease
- Rare genetic palpebral, lacrimal system and conjunctival disease
- Rare genetic parathyroid disease and phosphocalcic metabolism disorder
- Rare genetic parkinsonian disorder
- Rare genetic refraction anomaly
- Rare genetic renal disease
- Rare genetic respiratory disease
- Rare genetic skin disease
- Rare genetic systemic or rheumatologic disease
- Rare genetic thyroid disease
- Rare genetic tremor disorder
- Rare genetic tumor
- Rare genetic urogenital disease
- Rare genetic vascular disease
- Rare hemorrhagic disorder due to a constitutional coagulation factors defect
- Rare hemorrhagic disorder due to a constitutional platelet anomaly
- Rare hemorrhagic disorder due to a constitutional thrombocytopenia
- Rare hemorrhagic disorder due to a platelet receptor defect
- Rare hereditary ataxia
