Experimental Factor Ontology
2761 terms(s) returned
| Term Type: | Record: 801 to 850 of 2761 Records | Page: 17 of 56, First Previous Next Last | Show Records Per Page |
- 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
- Rare hereditary disease with avascular necrosis
- Rare hereditary disease with peripheral neuropathy
- Rare hereditary hemochromatosis
- Rare hereditary metabolic disease with peripheral neuropathy
- Rare hereditary neurologic disease with peripheral neuropathy
- Rare hereditary systemic disease with peripheral neuropathy
- Rare hereditary thrombophilia
- Rare hyperlipidemia
- Rare hyperopia and astigmatism
- Rare hyperthyroidism
- Rare hypolipidemia
- Rare hypothyroidism
- Rare insulin-resistance syndrome
- Rare intellectual disability without developmental anomaly
- Rare isolated myopia
- Rare lacrimal system disease
- Rare male infertility due to adrenal disorder of genetic origin
- Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
- Rare male infertility due to testicular endocrine disorder
- Rare metabolic liver disease
- Rare non-syndromic cataract
- Rare odontal or periodontal disorder
- Rare otorhinolaryngological malformation
- Rare palpebral disease
- Rare parkinsonian syndrome due to genetic neurodegenerative disease
- Rare paroxysmal movement disorder
- Rare pervasive developmental disorder
- Rare strabismus and restriction syndrome
- Rare syndrome with cardiac malformations
- Rare syndromic dyslipidemia
