skip to main content

Biological Sciences and Healthcare, part 4

Content language

Contact us: CRM@email.irandoc.ac.ir

Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency

Preferred term

Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency  

Type

  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

Broader concept

Has interpretation

Interprets

Is a

Occurrence

Pathological process

In other languages

URI

http://www.irandoc.acir/onto/irandoc/783200000

Download this concept:

RDF/XML TURTLE JSON-LD