Mondo Disease Ontology
181 terms(s) returned
| Term Type: | Record: 1 to 50 of 181 Records | Page: 1 of 4, First Previous Next Last | Show Records Per Page |
- X inactivation, familial skewed
- X inactivation, familial skewed, 1
- X inactivation, familial skewed, 2
- X small rings
- X-linked Alport syndrome
- X-linked Ehlers-Danlos syndrome
- X-linked Emery-Dreifuss muscular dystrophy
- X-linked Mendelian susceptibility to mycobacterial diseases
- X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
- X-linked Opitz G/BBB syndrome
- X-linked acrogigantism due to Xq26 microduplication
- X-linked adrenal hypoplasia congenita
- X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
- X-linked calvarial hyperostosis
- X-linked central congenital hypothyroidism with late-onset testicular enlargement
- X-linked cerebellar ataxia
- X-linked cerebral adrenoleukodystrophy
- X-linked cerebral-cerebellar-coloboma syndrome syndrome
- X-linked chondrodysplasia punctata
- X-linked chondrodysplasia punctata 1
- X-linked chondrodysplasia punctata 2
- X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome
- X-linked complex neurodevelopmental disorder
- X-linked complicated corpus callosum dysgenesis
- X-linked complicated spastic paraplegia type 1
- X-linked cone dysfunction syndrome with myopia
- X-linked cone-rod dystrophy
- X-linked cone-rod dystrophy 1
- X-linked cone-rod dystrophy 2
- X-linked cone-rod dystrophy 3
- X-linked congenital generalized hypertrichosis
- X-linked congenital hemolytic anemia
- X-linked congenital stationary night blindness
- X-linked corneal dermoid
- X-linked deafness
- X-linked diffuse leiomyomatosis-Alport syndrome
- X-linked disease
- X-linked disease, non-human animal
- X-linked distal spinal muscular atrophy type 3
- X-linked dominant chondrodysplasia, Chassaing-Lacombe type
- X-linked dominant disease
- X-linked dominant hypophosphatemic rickets
- X-linked dominant intellectual disability-epilepsy syndrome
- X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
- X-linked dystonia-parkinsonism
- X-linked endothelial corneal dystrophy
- X-linked erythropoietic protoporphyria
- X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome
- X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability
- X-linked hereditary sensory and autonomic neuropathy with hearing loss
