Mondo Disease Ontology
5944 terms(s) returned
| Term Type: | Record: 851 to 900 of 5944 Records | Page: 18 of 119, First Previous Next Last | Show Records Per Page |
- obsolete T-complex locus TCP10B
- obsolete TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome
- obsolete TUBB2A-related tubulinopathy
- obsolete Takayasu's arteritis
- obsolete Testicular dysgenesis
- obsolete Timothy grass allergy
- obsolete Tl antigen
- obsolete Torg-Winchester syndrome
- obsolete Trichohepatoenteric syndrome
- obsolete UV-damage excision repair, DNA incision
- obsolete Unicervical bicornuate uterus
- obsolete Usher syndrome type 1J
- obsolete Usher syndrome, type 2b
- obsolete VACTERL association
- obsolete VIPoma
- obsolete Vagneur-Triolle-Ripert syndrome
- obsolete Venezuelan hemorrhagic fever
- obsolete Vogt-Koyanagi-Harada disease
- obsolete WHIM syndrome
- obsolete Waldenstroem's macroglobulinemia
- obsolete Waldenstrom macroglobulinemia
- obsolete Walker-Warburg syndrome
- obsolete Walker-Warburg syndrome
- obsolete Waterhouse-Friderichsen syndrome
- obsolete Weissenbacher-Zweymuller syndrome
- obsolete West Nile encephalitis
- obsolete West syndrome
- obsolete Whipple disease
- obsolete Wilms tumor
- obsolete Wilms tumor
- obsolete Wiskott-Aldrich syndrome
- obsolete Wiskott-Aldrich syndrome
- obsolete Wolffian duct adenoma
- obsolete Wolman disease
- obsolete Wolman disease with hypolipoproteinemia and acanthocytosis
- obsolete Worth syndrome
- obsolete X and Y chromosomal anomaly
- obsolete X chromosome number anomaly
- obsolete X chromosome number anomaly with female phenotype
- obsolete X chromosome number anomaly with male phenotype
- obsolete X-linked B cell surface antigen, mouse, homolog-like 1
- obsolete X-linked acrogigantism due to a point mutation
- obsolete X-linked cleft palate and ankyloglossia
- obsolete X-linked complex spastic paraplegia
- obsolete X-linked congenital disorder of glycosylation with intellectual disability as a major feature
- obsolete X-linked distal hereditary motor neuropathy
- obsolete X-linked intellectual disability due to GRIA3 anomalies
- obsolete X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome
- obsolete X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome
- obsolete X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
