Concept information
Preferred term
X-linked recessive hereditary disease
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- FLNA-related X-linked myxomatous valvular dysplasia
- Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
- Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome (disorder)
- Juberg Marsidi syndrome (disorder)
- Lowe syndrome
- Macrocephaly, intellectual disability, left ventricular non compaction syndrome (disorder)
- Monocarboxylate transporter 8 deficiency
- Pelizaeus-Merzbacher disease in female carrier
- PLP1 null syndrome
- X-linked Emery-Dreifuss muscular dystrophy
- X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome (disorder)
- X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome
- X-linked intellectual disability hypotonic face syndrome
- X-linked lymphoproliferative syndrome
- X-linked mendelian susceptibility to mycobacterial disease (disorder)
- X-linked mental retardation syndrome, Christianson type
- X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder)
- X-linked moesin-associated immunodeficiency
- X-linked myopathy with postural muscle atrophy (disorder)
- X-linked spastic paraplegia type 16 (disorder)
- X-linked spastic paraplegia type 34
- X-linked thrombocytopenia with normal platelets (disorder)
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/1162976004
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}