Comparative

Human disease

short-rib thoracic dysplasia 14 with polydactyly

MONDO:0014688

Mondo defines it as: “An asphyxiating thoracic dystrophy that has material basis in homozygous mutation in the KIAA0586 gene on chromosome 14q23.”

1 disease group in OMIA reaches this disease, through OMIA's own Mondo link or its OMIM numbers. The page shows the chain. It does not say whether an animal is a model of this disease.

Animal diseases

By natural-model score for this disease, highest first. The score says how complete and how well supported each chain is, by stated rules. How the score works.

OMIA group Name Found by Species The chain reached Score
979 Talpid-3 OMIA's OMIM numbers 1 Target evidence 55.5

Human genes

Each human gene of these disease groups that Open Targets links to this disease.

Human gene Score Evidence
KIAA0586 0.76 1,322

Drugs tested for this disease

Each ChEMBL drug that has been tested for this disease, and the human genes above it acts on, if any. Open Targets gives some drugs, such as most enzyme replacement therapies, no target gene.

No drug has been tested for this disease.