Experimental Factor Ontology
11113 terms(s) returned
| Term Type: | Record: 3301 to 3350 of 11113 Records | Page: 67 of 223, First Previous Next Last | Show Records Per Page |
- obsolete_X-linked intellectual disability, Cilliers type
- obsolete_X-linked intellectual disability, Golabi-Ito-hall type
- obsolete_X-linked intellectual disability, Kroes type
- obsolete_X-linked intellectual disability, Miles-Carpenter type
- obsolete_X-linked intellectual disability, Pai type
- obsolete_X-linked intellectual disability, Porteous type
- obsolete_X-linked intellectual disability, Schimke type
- obsolete_X-linked intellectual disability, Schutz type
- obsolete_X-linked intellectual disability, Seemanova type
- obsolete_X-linked intellectual disability, Stevenson type
- obsolete_X-linked intellectual disability, Stocco dos Santos type
- obsolete_X-linked intellectual disability, Stoll type
- obsolete_X-linked intellectual disability, Sutherland-Haan type
- obsolete_X-linked intellectual disability, van Esch type
- obsolete_X-linked intellectual disability-retinitis pigmentosa syndrome
- obsolete_X-linked lethal multiple pterygium syndrome
- obsolete_X-linked lissencephaly with abnormal genitalia
- obsolete_X-linked mandibulofacial dysostosis
- obsolete_X-linked mendelian susceptibility to mycobacterial diseases
- obsolete_X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
- obsolete_X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
- obsolete_X-linked myopathy with excessive autophagy
- obsolete_X-linked myopathy with postural muscle atrophy
- obsolete_X-linked neurodegenerative syndrome, Bertini type
- obsolete_X-linked neurodegenerative syndrome, Hamel type
- obsolete_X-linked non progressive cerebellar ataxia
- obsolete_X-linked non-syndromic sensorineural deafness type DFN
- obsolete_X-linked osteoporosis with fractures
- obsolete_X-linked parkinsonism-spasticity syndrome
- obsolete_X-linked progressive cerebellar ataxia
- obsolete_X-linked pure spastic paraplegia
- obsolete_X-linked recessive ocular albinism
- obsolete_X-linked recessive optic atrophy
- obsolete_X-linked retinal dysplasia
- obsolete_X-linked retinoschisis
- obsolete_X-linked severe congenital neutropenia
- obsolete_X-linked sideroblastic anemia
- obsolete_X-linked sideroblastic anemia with ataxia
- obsolete_X-linked spinocerebellar ataxia type 3
- obsolete_X-linked spinocerebellar ataxia type 4
- obsolete_X-linked spondyloepimetaphyseal dysplasia
- obsolete_X-linked syndromic intellectual disability
- obsolete_XYLT1-CDG
- obsolete_Xp22.13p22.2 duplication syndrome
- obsolete_Xp22.3 microdeletion syndrome
- obsolete_Xq12-q13.3 duplication syndrome
- obsolete_Xq27.3q28 duplication syndrome
- obsolete_Y chromosome number anomaly
- obsolete_YAPC
- obsolete_Yellow Nail Syndrome
