Hydrops fetalis

Symptom Information:

Symptom ID: HPO:0001789
Synonyms:
Hydrops fetalis (disorder) [Orphanet:55160]
Hydrops Fetalis [Orphanet:55160]
Hydrops fetalis [OMIM:Hydrops fetalis]
Hydrops fetalis [Orphanet:55160]
Hydrops foetalis [Orphanet:55160]
Hydrops foetalis [MedDRA:10020529]
Hydrops fetalis [MedDRA:10020529]
Hydrops fetalis due to isoimmunization [MedDRA:10020529]
Hydrops fetalis not due to isoimmunization [MedDRA:10020529]
Hydrops foetalis due to isoimmunisation [MedDRA:10020529]
Hydrops foetalis not due to isoimmunisation [MedDRA:10020529]
Hydrops fetalis (type II, congenital) [OMIM:Hydrops fetalis (type II, congenital)]
Quality:
Cross references:
Orphanet:55160 "Hydrops fetalis" [Orphanet:55160]
OMIM: "Hydrops fetalis" [OMIM:Hydrops fetalis]
OMIM: "Hydrops fetalis (type II, congenital)" [OMIM:Hydrops fetalis (type II, congenital)]
UMLS:C0020305 "Hydrops Fetalis" [Orphanet:55160]
Is a (Direct Parents):
HPO         Edema
HPO         Abnormality of prenatal development or birth
Orphanet Abnormality of prenatal development or birth
MedDRA Foetal complications NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of fluid regulation(HPO:0011032)
             Edema(HPO:0000969)
                Hydrops fetalis(HPO:0001789)
       Abnormality of prenatal development or birth(HPO:0001197)
          Hydrops fetalis(HPO:0001789)
MedDRA:
Pregnancy, puerperium and perinatal conditions(MedDRA:10036585)
    Foetal complications(MedDRA:10016849)
       Foetal complications NEC(MedDRA:10016850)
          Hydrops fetalis(HPO:0001789)
Database Frequency: 63 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
Achondrogenesis type 1B (Orphanet:93298)
Achondrogenesis type 2 (Orphanet:93296)
Alpha-thalassemia (Orphanet:846)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Barth syndrome (Orphanet:111)
Boomerang dysplasia (Orphanet:1263)
CARDIAC VALVULAR DEFECT, DEVELOPMENTAL (OMIM:212093)
Campomelia, Cumming type (Orphanet:1318)
Cervicofacial lymphatic malformation (Orphanet:137923)
Chondrodysplasia, Blomstrand type (Orphanet:50945)
Congenital dyserythropoietic anemia type I (Orphanet:98869)
Congenital dyserythropoietic anemia type IV (Orphanet:293825)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Congenital pulmonary lymphangiectasia (Orphanet:2414)
Diffuse neonatal hemangiomatosis (Orphanet:2123)
Dysplastic cortical hyperostosis (Orphanet:2204)
Fetal Gaucher disease (Orphanet:85212)
Fetal parvovirus syndrome (Orphanet:295)
Fibrochondrogenesis (Orphanet:2021)
Free sialic acid storage disease (Orphanet:834)
Free sialic acid storage disease, infantile form (Orphanet:309324)
Gaucher disease (Orphanet:355)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Glycogen storage disease due to glycogen branching enzyme deficiency (Orphanet:367)
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form (Orphanet:308621)
HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES (OMIM:613124)
Hb Bart's hydrops fetalis (Orphanet:163596)
Hennekam syndrome (Orphanet:2136)
His bundle tachycardia (Orphanet:3283)
Hydrops fetalis (Orphanet:1041)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Idiopathic neonatal atrial flutter (Orphanet:45452)
Indomethacin embryofetopathy (Orphanet:1909)
Infantile Bartter syndrome with deafness (Orphanet:89938)
Klippel-Trénaunay syndrome (Orphanet:90308)
Left ventricular noncompaction 1 (OMIM:604169)
Lethal Kniest-like dysplasia (Orphanet:2347)
Lethal multiple pterygium syndrome (Orphanet:33108)
Mitochondrial trifunctional protein deficiency (Orphanet:746)
Mosaic trisomy 9 (Orphanet:99776)
Mucopolysaccharidosis type 7 (Orphanet:584)
Mycophenolate mofetil embryopathy (Orphanet:268249)
Neonatal hemochromatosis (Orphanet:446)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Phocomelia, Schinzel type (Orphanet:2879)
Platyspondylic dysplasia, Torrance type (Orphanet:85166)
Primary intestinal lymphangiectasia (Orphanet:90362)
Short rib-polydactyly syndrome, Majewski type (Orphanet:93269)
Short rib-polydactyly syndrome, Saldino-Noonan type (Orphanet:93270)
Short rib-polydactyly syndrome, Verma-Naumoff type (Orphanet:93271)
Short-rib thoracic dysplasia 6 with or without polydactyly (OMIM:263520)
Short-rib thoracic dysplasia 7 with or without polydactyly (OMIM:614091)
Sialidosis type 1 (Orphanet:812)
Sialidosis type 2 (Orphanet:87876)
Transaldolase deficiency (Orphanet:101028)
Trisomy 13 (Orphanet:3378)
Trisomy 1q (Orphanet:261344)
ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS (OMIM:276822)
Umbilical cord ulceration - intestinal atresia (Orphanet:3405)
Yunis-Varon syndrome (Orphanet:3472)