5801
|
|
|
Cytochrome c oxidase subunit 7A2 pseudogene 2 |
COX7A3, COX7AL, COX7AL2, COX7AP2 |
Curated: N/A
Unreviewed: N/A
|
5802
|
|
|
Cytochrome c oxidase subunit 7B |
APLCC, LSDMCA2 |
Curated: Microphthalmia, Mitochondrial disease, Linear skin defects with multiple congenital anomalies 2, Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism and other congenital anomalies, Microphthalmia with linear skin lesions, Linear skin defects with multiple congenital anomalies
Unreviewed: Absence Of Septum Pellucidum, Agenesis Of Corpus Callosum, Alzheimer disease, Ambiguous Genitalia, Aphasia, Aplasia Cutis Congenita, Atrial Septal Defect, Azoospermia, Bladder carcinoma, Cardiomyopathy, Cataract, Colpocephaly, Congenital Anomaly Of Rectum, Congenital Coloboma Of Iris, Congenital diaphragmatic hernia, Developmental Delay, Dwarfism, Dysphasia, Epispadias, Esophageal neoplasm, Esophageal squamous cell carcinoma, Glaucoma, Heart disease, Heart Septal Defects, Histiocytoid Cardiomyopathy, Hydrocephalus, Hypercholesterolemia, Hyperlipoproteinemia, Hypertrophic cardiomyopathy, Hypertrophy Of Clitoris, Hypospadias, Imperforate anus, Linear Skin Defects With Multiple Congenital Anomalies, Male Pseudohermaphroditism, Malignant Neoplasm, Mandibular aplasia, Mental retardation, Microcephaly, Micrognathism, Microphthalmia With Linear Skin Defects Syndrome, Microphthalmos, Mitral Valve Prolapse, Nasopharyngeal Carcinoma, Overriding aorta, Ovotestis, Penis Agenesis, Posterior embryotoxon, Psoriatic arthritis, Respiratory Failure, Retinal Dysplasia, Retinal Dystrophy, Retinitis Pigmentosa, Sclerocornea, Skin Lesion, Specific Learning Disorder, Status Epilepticus, Syndromic microphthalmia, Tricuspid Valve Insufficiency, Tricuspid Valve Prolapse, True Hermaphroditism, Urinary bladder cancer, Urinary bladder neoplasms, Ventricular septal defect, Vitiligo, Vitritis
|
5803
|
|
|
Cytochrome c oxidase subunit 7B2 |
- |
Curated: Alzheimer disease, Hepatocellular carcinoma, Migraine
Unreviewed: Breast neoplasm, Liver carcinoma, Nasopharyngeal Carcinoma
|
5804
|
|
|
COX7B pseudogene 1 |
bK714B7.1 |
Curated: N/A
Unreviewed: N/A
|
5805
|
|
|
COX7B pseudogene 2 |
dJ901O8.2 |
Curated: N/A
Unreviewed: N/A
|
5806
|
|
|
COX7B pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
5807
|
|
|
COX7B pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
|
5808
|
|
|
COX7B pseudogene 6 |
- |
Curated: N/A
Unreviewed: N/A
|
5809
|
|
|
Cytochrome c oxidase subunit 7C |
- |
Curated: Obesity
Unreviewed: Alzheimer disease, Cognition disorder, Dementia, Diabetes mellitus, type 1, Fatigue syndrome, Peritonitis, Venous thromboembolism
|
5810
|
|
|
COX7C pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|