Stillbirth
Symptom Information:
Symptom ID: | HPO:0003826 | |||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: Pregnancy, puerperium and perinatal conditions(MedDRA:10036585) Abortions and stillbirth(MedDRA:10000211) Stillbirth and foetal death(MedDRA:10053173) Stillbirth(HPO:0003826) |
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Database Frequency: | 40 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Achondrogenesis | (Orphanet:932) |
Achondrogenesis type 1B | (Orphanet:93298) |
Achondrogenesis type 2 | (Orphanet:93296) |
Acromesomelic dysplasia, Grebe type | (Orphanet:2098) |
Atelosteogenesis type I | (Orphanet:1190) |
Atelosteogenesis type II | (Orphanet:56304) |
Barth syndrome | (Orphanet:111) |
CHILD syndrome | (Orphanet:139) |
Cervicofacial lymphatic malformation | (Orphanet:137923) |
Chondrodysplasia, Blomstrand type | (Orphanet:50945) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
FETAL AKINESIA SYNDROME, X-LINKED | (OMIM:300073) |
Fetal Gaucher disease | (Orphanet:85212) |
Fetal akinesia deformation sequence | (Orphanet:994) |
Fibrochondrogenesis | (Orphanet:2021) |
Fryns syndrome | (Orphanet:2059) |
Gaucher disease type 2 | (Orphanet:77260) |
Greenberg dysplasia | (Orphanet:1426) |
HEMOGLOBIN--ZETA LOCUS | (OMIM:142310) |
Hydrolethalus | (Orphanet:2189) |
Infantile osteopetrosis with neuroaxonal dysplasia | (Orphanet:85179) |
Intestinal lymphangiectasia | (Orphanet:36204) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Meckel syndrome, type 2 | (OMIM:603194) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Neonatal hemochromatosis | (Orphanet:446) |
Neu-Laxova syndrome | (Orphanet:2671) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Otopalatodigital syndrome | (Orphanet:669) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Polysyndactyly - cardiac malformation | (Orphanet:2934) |
Pyknoachondrogenesis | (Orphanet:3003) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 2 | (OMIM:615415) |
Roberts syndrome | (Orphanet:3103) |
Schneckenbecken dysplasia | (Orphanet:3144) |
Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
THYMIC APLASIA WITH FETAL DEATH | (OMIM:274210) |
Tetrasomy 12p | (Orphanet:884) |
VACTERL with hydrocephalus | (Orphanet:3412) |