Disease association ontology term - MONDO:0020811 - mitochondrial complex III deficiency, nuclear type
Term summary
ID
MONDO:0020811
Name
mitochondrial complex III deficiency, nuclear type
Ontology or CV name
Disease association
Parents
is_a
mitochondrial complex III deficiency
Annotation
Disease association
MONDO:0007415
-
mitochondrial complex III deficiency nuclear type 1
References:
PB_REF:0000006
Genes:
bcs1 (SPAC644.07)
MONDO:0014063
-
mitochondrial complex III deficiency nuclear type 2
References:
PB_REF:0000006
Genes:
mgr3 (SPAP27G11.02)
MONDO:0014064
-
mitochondrial complex III deficiency nuclear type 3
References:
PB_REF:0000006
Genes:
qcr7 (SPCC737.02c)
MONDO:0014065
-
mitochondrial complex III deficiency nuclear type 4
References:
PB_REF:0000006
Genes:
qcr8 (SPAC1782.07)
MONDO:0014066
-
mitochondrial complex III deficiency nuclear type 5
References:
PB_REF:0000006
Genes:
qcr2 (SPCC613.10)
MONDO:0014194
-
mitochondrial complex III deficiency nuclear type 6
References:
PB_REF:0000006
Genes:
cyt1 (SPBC29A3.18)
MONDO:0014356
-
mitochondrial complex III deficiency nuclear type 7
References:
PB_REF:0000006
Genes:
cbp6 (SPBC947.14c)
MONDO:0014364
-
mitochondrial complex III deficiency nuclear type 8
References:
PB_REF:0000006
Genes:
mzm1 (SPBC30D10.21)
MONDO:0014496
-
mitochondrial complex III deficiency nuclear type 9
References:
PB_REF:0000006
PMID:25008109
Genes:
cbp4 (SPBC27B12.14)
MONDO:0032909
-
mitochondrial complex III deficiency, nuclear type 10
References:
PB_REF:0000006
Genes:
rip1 (SPBC16H5.06)
MONDO:0859321
-
mitochondrial complex III deficiency, nuclear type 11
References:
PB_REF:0000006
Genes:
qcr6 (SPBC16C6.08c)