asphyxiating thoracic dystrophy 2
asphyxiating thoracic dystrophy that has material basis in homozygous mutation in the IFT80 gene on chromosome 3q25
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asphyxiating thoracic dystrophy 2
Summary
asphyxiating thoracic dystrophy 2 is a rare disease[1]. It is known by 6 alternative names across languages and contexts.[2]
Key Facts
- asphyxiating thoracic dystrophy 2's instance of is recorded as rare disease[3].
- asphyxiating thoracic dystrophy 2's instance of is recorded as class of disease[4].
- asphyxiating thoracic dystrophy 2 is a type of asphyxiating thoracic dysplasia[5].
- asphyxiating thoracic dystrophy 2 is a type of autosomal recessive disease[6].
- asphyxiating thoracic dystrophy 2's health specialty is recorded as medical genetics[7].
- asphyxiating thoracic dystrophy 2's genetic association is recorded as IFT80[8].
- asphyxiating thoracic dystrophy 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110086[9].
- asphyxiating thoracic dystrophy 2's exact match is recorded as http://identifiers.org/doid/DOID:0110086[10].
- asphyxiating thoracic dystrophy 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
asphyxiating thoracic dystrophy 2 is known by 6 alternative names across languages and contexts.[2]