NORD^® Rare Disease Database

hydrops fetalis

Also known as: HF, familial non-immune hydrops fetalis, fetal anasarca, fetal edema, fetal hydrops, foetal anasarca, foetal hydrops, foetal oedema, generalised foetal oedema, generalized fetal edema, hydrops fetalis, hydrops fetalis (disease), hydrops fetalis nonimmune, idiopathic hydrops fetalis

non-immune hydrops fetalis

Also known as: Haemoglobin H hydrops fetalis syndrome, Hemoglobin H hydrops fetalis syndrome, NIHF, hydrops fetalis, Alpha-thalassemia-related, hydrops fetalis, nonimmune, non-immune HF, non-immune fetal edema, non-immune fetal hydrops, non-immune foetal hydrops, non-immune foetal oedema

well-differentiated fetal adenocarcinoma of the lung

Also known as: WDFA, fetal adenocarcinoma, fetal lung adenocarcinoma, foetal adenocarcinoma, foetal lung adenocarcinoma, pulmonary adenocarcinoma of fetal type, pulmonary adenocarcinoma of foetal type, pulmonary endodermal tumor resembling fetal lung, pulmonary endodermal tumour resembling foetal lung, well-differentiated fetal lung adenocarcinoma, well-differentiated foetal lung adenocarcinoma

hereditary persistence of fetal hemoglobin

Also known as: Disease, Haemoglobin F, Disease, Hemoglobin F, HEMOGLOBIN F DIS, HPFH - Hereditary persistence of fetal hemoglobin, HPFH - Hereditary persistence of foetal haemoglobin, Haemoglobin F Disease, Hb F disease, Hemoglobin F Disease, Hereditary Persistence of Fetal Hemoglobin, Hereditary Persistence of Foetal Haemoglobin, Hereditary persistence of fetal hemoglobin, Hereditary persistence of foetal haemoglobin, hereditary persistence of fetal hemoglobin

fetal akinesia deformation sequence

Also known as: FADS, arthrogryposis multiplex congenita with pulmonary hypoplasia, arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome, fetal akinesia deformation sequence, fetal akinesia sequence, foetal akinesia sequence

Hb Bart’s hydrops fetalis

Also known as: Alpha-thalassemia major, HBA1;HBA2 digenic quadallelic Hb Bart’s hydrops fetalis, Haemoglobin Bart's hydrops fetalis, Hb Bart’s hydrops fetalis caused by quadallelic variation in HBA1;HBA2, Hb Bart’s hydrops fetalis related to quadallelic variation in HBA1 and HBA2, Hemoglobin Bart's hydrops fetalis, alpha-thalassemia hydrops fetalis, homozygous alpha0-thalassemia

immune hydrops fetalis

Also known as: IHF, immune HF, immune fetal edema, immune fetal hydrops, immune foetal hydrops, immune foetal oedema

EPHB4-related lymphatic-related hydrops fetalis

Also known as: EPHB4-related LRHF/GLD, EPHB4-related generalised lymphatic dysplasia with atrial septal defect, EPHB4-related generalised lymphatic dysplasia with non-immune hydrops fetalis, EPHB4-related generalized lymphatic dysplasia with atrial septal defect, EPHB4-related generalized lymphatic dysplasia with non-immune hydrops fetalis

fetal iodine syndrome

Also known as: FIDD, endemic cretinism, fetal iodine deficiency disorder, foetal iodine deficiency disorder

PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis

Also known as: PIEZO1-related LRHF/GLD, PIEZO1-related generalised lymphatic dysplasia with systemic involvement, PIEZO1-related generalized lymphatic dysplasia with systemic involvement, PIEZO1-related lymphatic-related hydrops fetalis, generalised lymphatic dysplasia of Fotiou, generalized lymphatic dysplasia of Fotiou

fetal erythroblastosis

Also known as: EF - erythroblastosis foetalis, HDFN, erythroblastosis fetalis, haemolytic disease due to rhesus isoimmunisation, hemolytic disease of the fetus or newborn, hemolytic disease of the foetus or newborn, hemolytic disease of the newborn, isoimmune hemolytic disease of the newborn, rhesus isoimmunisation of the newborn

fetal akinesia-cerebral and retinal hemorrhage syndrome

Also known as: LCCS5, lethal congenital contracture syndrome 5, lethal congenital contracture syndrome type 5, myopathy, centronuclear, lethal, autosomal recessive

lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome

Also known as: MKS12, Meckel syndrome 12, Meckel syndrome type 12

hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome

Also known as: HPFH-beta-thalassemia syndrome

lissencephaly type 3-familial fetal akinesia sequence syndrome

fetal trimethadione syndrome

sporadic fetal brain disruption sequence

fetal minoxidil syndrome

Also known as: minoxidil antenatal exposure, minoxidil antenatal infection

hereditary persistence of fetal hemoglobin-sickle cell disease syndrome

Also known as: HPFH-sickle cell disease syndrome

fetal akinesia deformation sequence 1

Also known as: FADS1, Pena-Shokeir syndrome type 1, Pena-Shokeir syndrome, type 1

fetal akinesia deformation sequence 2

Also known as: FADS2

fetal akinesia deformation sequence 3

Also known as: FADS3

fetal akinesia deformation sequence 4

Also known as: FADS4

fetal carbamazepine syndrome