RLIM, ring finger protein, LIM domain interacting, 51132
N. diseases: 64; N. variants: 8
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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
phenotype | Finding | 477 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | Congenital Abnormality | 127 | 83 | 0.100 | None | 0 | 1 | |||||||
|
disease | Acquired Abnormality | 27 | 2 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Male Urogenital Diseases | Congenital Abnormality | 217 | 11 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 75 | 24 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | Congenital Abnormality | 366 | 80 | 0.100 | None | 0 | ||||||||
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disease | Mental or Behavioral Dysfunction | 1825 | 553 | 0.100 | None | 0 | 1 | ||||||||
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phenotype | Behavior and Behavior Mechanisms | Finding | 560 | 192 | 0.100 | None | 0 | 1 | |||||||
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phenotype | Finding | 67 | 11 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 125 | 8 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 70 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 89 | 11 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 69 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 87 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 39 | 3 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases | Finding | 13 | 1 | 0.100 | None | 0 | 1 | |||||||
|
phenotype | Finding | 1010 | 0.100 | None | 0 | ||||||||||
|
phenotype | Anatomical Abnormality | 122 | 14 | 0.100 | None | 0 | |||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 955 | 164 | 0.100 | None | 0 | ||||||||
|
disease | Anatomical Abnormality | 190 | 12 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 149 | 5 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 180 | 8 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 429 | 29 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 133 | 13 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 208 | 9 | 0.100 | None | 0 |