HomoeOmicsDB
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Autonomic Nervous System Imbalance
Autosomal Dominant Hypocalcemia
Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Macrothrombocytopenia
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
Autosomal Dominant Osteopetrosis
Autosomal Dominant Parkinsonism
Autosomal Dominant Retinitis Pigmentosa
Autosomal Recessive Agammaglobulinemia
Autosomal Recessive Limb Girdle Muscular Dystrophy Type 2B
Autosomal Recessive Osteopetrosis
Autosomal Recessive Parkinsonism
Autosomal Recessive Polycystic Kidney Disease
Autosomal Recessive Primary Microcephaly
Avascular Necrosis Of Femoral Head, Primary, 1
Avascular Necrosis Of Femoral Head, Primary, 2
Avascular Necrosis Of The Capital Femoral Epiphysis
Avascular Retina
Avellino Corneal Dystrophy
Avitaminosis
Awakening Epilepsy
Axenfeld Anomaly (Disorder)
Axenfeld Syndrome
Axenfeld-Rieger Syndrome
Axenfeld-Rieger Syndrome, Type 1
Axenfeld-Rieger Syndrome, Type 3
Axial Spondyloarthritis
Axonal Neuropathy
Axonal Sensorimotor Neuropathy
Azoospermia
Azoospermia, Nonobstructive
B Acute Lymphoblastic Leukemia With T(9;22)(Q34.1;Q11.2); Bcr-Abl1
B Lymphoblastic Leukemia Lymphoma, No Icd-O Subtype
B Lymphoblastic Lymphoma
B-Cell Aplasia
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