← Назад

Severe congenital hypochromic anemia with ringed sideroblasts

ORPHA:300298DiseaseUnknownInfancy, Neonatal

Ассоциированные гены (1)

STEAP3
STEAP3 metalloreductase
Disease-causing germline mutation(s) in
OMIM: 609671

Фенотипы (20)

Очень частый (80–99%)4
HP:0001896Reticulocytopenia
HP:0001903Anemia
HP:0003281Increased circulating ferritin concentration
HP:0012464Decreased transferrin saturation
Частый (30–79%)10
HP:0000027Azoospermia
HP:0000135Hypogonadism
HP:0000864Abnormality of the hypothalamus-pituitary axis
HP:0000980Pallor
HP:0002910Elevated circulating hepatic transaminase concentration
HP:0003452Increased serum iron
HP:0004823Anisopoikilocytosis
HP:0012378Fatigue
HP:0012465Elevated hepatic iron concentration
HP:0025066Decreased mean corpuscular volume
Периодический (5–29%)6
HP:0000821Hypothyroidism
HP:0000846Adrenal insufficiency
HP:0000957Cafe-au-lait spot
HP:0001433Hepatosplenomegaly
HP:0001510Growth delay
HP:0012134Dysplastic erythropoesis

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
<1 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы