Source: HPO

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C0268731
Disease: Renal glomerular disease
Renal glomerular disease 		group 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes 		disease 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		disease 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency 		disease 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas 		disease 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C3203102
Disease: Idiopathic pulmonary arterial hypertension
Idiopathic pulmonary arterial hypertension 		disease 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C3714745
Disease: Malabsorption
Malabsorption 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C4021734
Disease: Abnormality of mitochondrial metabolism
Abnormality of mitochondrial metabolism 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures 		disease 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C4022012
Disease: Death in early adulthood
Death in early adulthood 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality 		disease 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C4025821
Disease: Anterior hypopituitarism
Anterior hypopituitarism 		disease 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C4520679
Disease: Abnormal macular morphology
Abnormal macular morphology 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		disease 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C2973725
Disease: Pulmonary arterial hypertension
Pulmonary arterial hypertension 		disease 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C1836735
Disease: hypopigmented skin patch
hypopigmented skin patch 		phenotype 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C1836830
Disease: Developmental regression
Developmental regression 		disease 0.100 None 0 0
Entrez Id: 4564
Gene Symbol: TRNH
TRNH 		tRNA 0.597 0.731
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		disease 0.100 None 0 0