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Showing 7,221-7,240 of 10,888 diseases
MONDO:0033483
Erythrocytosis, familial, 5 is a form of familial polycythemia that arises from a mutation in the EPO gene, a key regulator of red blood cell producti...
MONDO:0054801
MONDO:0054802
Familial erythrocytosis, familial, 7 is a genetic condition characterized by an increase in red blood cell production linked to changes in the alpha-g...
MONDO:0017787
MONDO:0020703
Erythroid neoplasm is a type of malignant tumor that arises from the erythroid lineage of blood cells. Research has implicated abnormalities in the JA...
MONDO:0019270
Erythrokeratoderma is an umbrella term for a group of rare genetic skin disorders marked by well-demarcated plaques of reddened, dry, and thickened sk...
MONDO:0017836
MONDO:0017851
Erythrokeratodermia variabilis is a rare genetic chronic skin disorder characterized by hyperkeratosis and transient erythema. It primarily affects th...
MONDO:0033010
Erythrokeratodermia variabilis et progressiva 1 is a genetic skin condition primarily characterized by persistent redness and thickening of the skin....
MONDO:0033012
MONDO:0033013
MONDO:0033014
MONDO:0033015
MONDO:0032801
MONDO:0030941
MONDO:0859598
MONDO:0007573
MONDO:0001676
Erythropoietic protoporphyria is a rare congenital metabolic disorder resulting from an inborn error in the porphyrin-heme biosynthesis pathway. The c...
MONDO:0017231
MONDO:0002440
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