Experimental Factor Ontology
11113 terms(s) returned
| Term Type: | Record: 1051 to 1100 of 11113 Records | Page: 22 of 223, First Previous Next Last | Show Records Per Page |
- obsolete rare genetic bone development disorder
- obsolete rare genetic disease with myoclonus as a major feature
- obsolete rare genetic disorder with obstructive azoospermia
- obsolete rare genetic hypothalamic or pituitary disease
- obsolete rare genetic parathyroid disease and phosphocalcic metabolism disorder
- obsolete rare genetic refraction anomaly
- obsolete rare hemorrhagic disorder due to a constitutional coagulation factors defect
- obsolete rare hereditary disease with avascular necrosis
- obsolete rare hereditary disease with peripheral neuropathy
- obsolete rare hereditary metabolic disease with peripheral neuropathy
- obsolete rare hereditary neurologic disease with peripheral neuropathy
- obsolete rare hereditary systemic disease with peripheral neuropathy
- obsolete rare hereditary thrombophilia
- obsolete rare hyperopia and astigmatism
- obsolete rare insulin-resistance syndrome
- obsolete rare male infertility due to adrenal disorder of genetic origin
- obsolete rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
- obsolete rare male infertility due to testicular endocrine disorder
- obsolete rare odontal or periodontal disorder
- obsolete rare otorhinolaryngological malformation
- obsolete rare parkinsonian syndrome due to genetic neurodegenerative disease
- obsolete rare paroxysmal movement disorder
- obsolete rare strabismus and restriction syndrome
- obsolete rare syndrome with cardiac malformations
- obsolete recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome
- obsolete reproduction
- obsolete resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta
- obsolete resistance to thyrotropin-releasing hormone syndrome
- obsolete respiratory malformation
- obsolete respiratory or mediastinal malformation
- obsolete response to paclitaxel
- obsolete retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene
- obsolete ribonucleoside monophosphate metabolic process
- obsolete ribonucleoside triphosphate metabolic process
- obsolete ring chromosome
- obsolete secondary dysgenetic glaucoma
- obsolete secondary ectropion
- obsolete secondary entropion
- obsolete secretory apparatus of the lacrimal system anomaly
- obsolete semilobar holoprosencephaly
- obsolete septopreoptic holoprosencephaly
- obsolete serine family amino acid metabolic process
- obsolete severe COVID-19 infection
- obsolete severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome
- obsolete severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency
- obsolete short rib-polydactyly syndrome, Saldino-Noonan type
- obsolete short rib-polydactyly syndrome, Verma-Naumoff type
- obsolete short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies
- obsolete short stature-delayed bone age due to thyroid hormone metabolism deficiency
- obsolete sickle cell disease and related diseases
