|
91
|
|
|
ADAM metallopeptidase domain 30 |
svph4 |
|
|
92
|
|
|
ADAM metallopeptidase domain 29 |
CT73, svph1 |
|
|
93
|
|
|
Aldo-keto reductase family 1 member C4 |
3-alpha-HSD, C11, CDR, CHDR, DD-4, DD4, HAKRA |
|
|
94
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 13 |
ADAM-TS13, ADAMTS-13, C9orf8, VWFCP, vWF-CP |
Achoo syndrome, Anemia, Congenital thrombotic thrombocytopenic purpura, Hemolytic uremic syndrome, Immune thrombocytopenic purpura, Ischemic stroke, Liver carcinoma, Microangiopathic hemolytic anemia, Petechiae, Thrombotic microangiopathies, Thrombotic thrombocytopenic purpura |
|
95
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 8 |
ADAM-TS8, METH2 |
|
|
96
|
|
|
Adenylate cyclase 5 |
AC5, DSKOD, FDFM |
Anaplastic carcinoma, Anxiety disorder, Benign hereditary chorea, Carcinoma, Cardiomyopathy, Chorea, Chronic obstructive pulmonary disease, Cirrhosis, Congestive heart failure, Developmental delay, Diabetes mellitus, Dysarthria, Dyskinesia and facial myokymia, Dyskinesia, with facial myokymia, Dyskinetic syndrome, Dysmorphic features, Hypertension, Orofacial dyskinesia, Mental depression, Movement disorders, Myocardial diseases, Neurodevelopmental disorders, OsteoporosisView all (8 more) |
|
97
|
|
|
Arginyltransferase 1 |
- |
|
|
98
|
|
|
Adaptor related protein complex 4 subunit sigma 1 |
AP47B, CLA20, CLAPS4, CPSQ6, SPG52 |
Cerebellar atrophy, Cerebral cortical atrophy, Cerebral palsy, Congenital clubfoot, Developmental dysplasia of the hip, Congenital genu recurvatum, Developmental delay, Dwarfism, Dysmorphic features, High palate, Hypoplasia of corpus callosum, Mental retardation, Macrostomia, Mental retardation with spastic paraplegia, Microcephaly, Spastic paraplegia, Stereotyped behavior, StrabismusView all (3 more) |
|
99
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 7 |
ADAM-TS 7, ADAM-TS7, ADAMTS-7 |
|
|
100
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 6 |
ADAM-TS 6, ADAM-TS6, ADAMTS-6 |
|
