Hydrops fetalis
Symptom Information:
Symptom ID: | HPO:0001789 | ||||||||||||
Synonyms: |
|
||||||||||||
Quality: | |||||||||||||
Cross references: |
|
||||||||||||
Is a (Direct Parents): |
|
||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of prenatal development or birth(HPO:0001197) Hydrops fetalis(HPO:0001789) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of fluid regulation(HPO:0011032) Edema(HPO:0000969) 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) |