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| created at |
2021-12-13 15:49:09 UTC |
| updated at |
2021-12-13 16:09:58 UTC |
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Mondo Disease Ontology (Mondo).
Mondo aims to harmonizes disease definitions across the world. For more details on this ontology see:
Mondo website: https://monarch-initiative.github.io/mondo
OBO Foundry Mondo page: http://obofoundry.org/ontology/mondo.html
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24,745 entries
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There is 0 pattern entry.
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X-linked epilepsy-learning disabilities-behavior disorders syndrome
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0010339 |
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X-linked erythropoietic protoporphyria
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0010420 |
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X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome
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0044702 |
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X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability
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0018821 |
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X-linked hereditary sensory and autonomic neuropathy with deafness
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0010378 |
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X-linked hydrocephalus with stenosis of the aqueduct of Sylvius
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0010611 |
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X-linked hypohidrotic ectodermal dysplasia
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0010585 |
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X-linked hypophosphatemic rickets
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0020720 |
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X-linked ichthyosis syndrome
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0017269 |
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X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
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0010455 |
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X-linked immunoneurologic disorder
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0010243 |
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X-linked intellectual disability
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0100284 |
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X-linked intellectual disability due to GRIA3 anomalies
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0018222 |
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X-linked intellectual disability with hypopituitarism
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0100195 |
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X-linked intellectual disability with isolated growth hormone deficiency
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0019032 |
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