ADAMTS10, ADAM metallopeptidase with thrombospondin type 1 motif 10, 81794
N. diseases: 67; N. variants: 12
Source: ALL
Disease | Type | Disease Class | Semantic Type | N. genes d | N. SNPs d | Score gda | EL gda | EI gda | N. PMIDs | N. SNPs gda | First Ref. | Last Ref. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
disease | Disease or Syndrome | 59 | 442 | 0.300 | limited | 0 | |||||||||
|
phenotype | Finding | 14 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 40 | 5 | 0.100 | None | 0 | |||||||||
|
disease | Musculoskeletal Diseases | Anatomical Abnormality | 92 | 8 | 0.100 | None | 0 | ||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases | Finding | 19 | 11 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | Disease or Syndrome | 393 | 34 | 0.100 | None | 0 | ||||||||
|
disease | Musculoskeletal Diseases | Congenital Abnormality | 49 | 3 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 3 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 13 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 1127 | 292 | 0.100 | None | 0 | |||||||||
|
disease | Eye Diseases | Disease or Syndrome | 184 | 116 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 12 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 7 | 0.100 | None | 0 | ||||||||||
|
disease | Anatomical Abnormality | 4 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | Finding | 115 | 6 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | Finding | 422 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Eye Diseases | Sign or Symptom | 235 | 11 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 1010 | 0.100 | None | 0 | ||||||||||
|
phenotype | Eye Diseases | Finding | 20 | 4 | 0.100 | None | 0 | ||||||||
|
disease | Musculoskeletal Diseases | Anatomical Abnormality | 35 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 84 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 22 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 18 | 0.100 | None | 0 | ||||||||||
|
disease | Musculoskeletal Diseases | Congenital Abnormality | 24 | 0.100 | None | 0 |