Mondo Disease Ontology
276 terms(s) returned
| Term Type: | Record: 101 to 150 of 276 Records | Page: 3 of 6, First Previous Next Last | Show Records Per Page |
- X-linked intellectual disability-seizures-psoriasis syndrome
- X-linked intellectual disability-short stature-overweight syndrome
- X-linked intellectual disability-spastic quadriparesis syndrome
- X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome
- X-linked lethal multiple pterygium syndrome
- X-linked lissencephaly with abnormal genitalia
- X-linked lymphoproliferative disease due to SH2D1A deficiency
- X-linked lymphoproliferative disease due to XIAP deficiency
- X-linked lymphoproliferative syndrome
- X-linked mandibulofacial dysostosis
- X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome
- X-linked mixed hearing loss with perilymphatic gusher
- X-linked myopathy with excessive autophagy
- X-linked myopathy with postural muscle atrophy
- X-linked myotubular myopathy
- X-linked myotubular myopathy-abnormal genitalia syndrome
- X-linked neurodegenerative syndrome, Bertini type
- X-linked neurodegenerative syndrome, Hamel type
- X-linked non progressive cerebellar ataxia
- X-linked nonsyndromic hearing loss
- X-linked osteoporosis with fractures
- X-linked paralytic tremor, PLP1-related, rabbit
- X-linked parkinsonism-spasticity syndrome
- X-linked progressive cerebellar ataxia
- X-linked progressive retinal atrophy 1, RPGR-related, dog
- X-linked progressive retinal atrophy 2, RPGR-related, dog
- X-linked progressive retinal atrophy, type 3, dog
- X-linked recessive disease
- X-linked recessive inheritance
- X-linked recessive mitochondrial myopathy
- X-linked recessive ocular albinism
- X-linked reticulate pigmentary disorder
- X-linked retinal dysplasia
- X-linked retinoschisis
- X-linked scapuloperoneal muscular dystrophy
- X-linked severe combined immunodeficiency disease, IL2RG-related, dog
- X-linked severe combined immunodeficiency disease, IL2RG-related, golden hamster
- X-linked severe combined immunodeficiency disease, IL2RG-related, pig
- X-linked severe congenital neutropenia
- X-linked severe syndromic thoracic aortic aneurysm and dissection
- X-linked sideroblastic anemia 1
- X-linked sideroblastic anemia with ataxia
- X-linked spasticity-intellectual disability-epilepsy syndrome
- X-linked spermatogenic failure 1
- X-linked spinocerebellar ataxia type 3
- X-linked spinocerebellar ataxia type 4
- X-linked spondyloepimetaphyseal dysplasia
- X-linked syndromic complex neurodevelopmental disorder
- X-linked syndromic intellectual disability
- XBP1
