Concept information
Preferred term
Autosomal hereditary disorder
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Adams-Oliver syndrome
- Adult hypophosphatasia
- alpha, alpha-Trehalase deficiency
- Central core disease
- Crigler-Najjar syndrome
- Distal arthrogryposis syndrome
- Dominant hereditary disorder, NOS
- Familial visceral neuropathy
- Hereditary spherocytosis
- HNSHA due to hexokinase deficiency
- Hypodysfibrinogenaemia
- Progressive cone-rod dystrophy
- Robinow syndrome
- Treacher Collins syndrome
- von Willebrand disease type 2
Is a
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/1899006
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