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Metadata
ID DOID:0111853
Name primary ciliary dyskinesia 40
Definition A primary ciliary dyskinesia characterized by a subtle defect in the bend of the distal portion of the cilia, reduced ciliary clearance in-vitro, relatively mild respiratory phenotype and laterality defects in all reported patients that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH9 gene on chromosome 17p12.
https://www.ncbi.nlm.nih.gov/pubmed/30471718, https://www.ncbi.nlm.nih.gov/pubmed/30471717
Xrefs

MIM:618300

Synonyms

CILD40 [EXACT]

primary ciliary dyskinesia 40 with or without situs inversus [EXACT]

Parent Relationships

is_a autosomal recessive disease

is_a primary ciliary dyskinesia

Subclass Logical Relationships

has material basis in some autosomal recessive inheritance

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