Neonatal death
Symptom Information:
Symptom ID: | HPO:0003811 | ||||||||
Synonyms: |
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Is a (Whole tree): |
HPO:
MedDRA: General disorders and administration site conditions(MedDRA:10018065) Fatal outcomes(MedDRA:10053172) Death and sudden death(MedDRA:10011907) Neonatal death(HPO:0003811) |
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Database Frequency: | 44 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Atelosteogenesis type I | (Orphanet:1190) |
Autosomal recessive polycystic kidney disease | (Orphanet:731) |
Boomerang dysplasia | (Orphanet:1263) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Congenital alveolar capillary dysplasia | (Orphanet:210122) |
Diabetic embryopathy | (Orphanet:1926) |
Dyssegmental dysplasia, Silverman-Handmaker type | (Orphanet:1865) |
EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA | (OMIM:226735) |
Familial primary pulmonary hypoplasia | (Orphanet:2257) |
Fetal Gaucher disease | (Orphanet:85212) |
Fibulo-ulnar hypoplasia - renal anomalies | (Orphanet:2256) |
GENITOURINARY TRACT ANOMALIES | (OMIM:305690) |
GRANULOMAS, CONGENITAL CEREBRAL | (OMIM:306300) |
Greenberg dysplasia | (Orphanet:1426) |
HERNIA, ANTERIOR DIAPHRAGMATIC | (OMIM:306950) |
Hypotonia with lactic acidemia and hyperammonemia | (Orphanet:137908) |
Lethal Larsen-like syndrome | (Orphanet:2371) |
Lethal acantholytic epidermolysis bullosa | (Orphanet:158687) |
Lethal arthrogryposis - anterior horn cell disease | (Orphanet:53696) |
Lethal chondrodysplasia, Seller type | (Orphanet:1421) |
Lethal congenital contracture syndrome type 1 | (Orphanet:1486) |
Lethal congenital contracture syndrome type 3 | (Orphanet:137783) |
Lethal faciocardiomelic dysplasia | (Orphanet:1972) |
Lethal infantile mitochondrial myopathy | (Orphanet:254857) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
Lung agenesis - heart defect - thumb anomalies | (Orphanet:1120) |
MEDIUM CHAIN 3-KETOACYL-CoA THIOLASE DEFICIENCY | (OMIM:602199) |
Marden-Walker syndrome | (Orphanet:2461) |
Meckel syndrome, type 4 | (OMIM:611134) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
NEUTROPENIA, LETHAL CONGENITAL, WITH EOSINOPHILIA | (OMIM:257100) |
Neonatal hemochromatosis | (Orphanet:446) |
Pallister-Hall syndrome | (Orphanet:672) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
Reticular dysgenesis | (Orphanet:33355) |
Short rib-polydactyly syndrome, Beemer-Langer type | (Orphanet:93268) |
THANATOPHORIC DYSPLASIA, GLASGOW VARIANT | (OMIM:273680) |
THANATOPHORIC DYSPLASIA, TYPE II | (OMIM:187601) |
Thanatophoric dysplasia type 1 | (Orphanet:1860) |
ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS | (OMIM:276822) |
Ulbright-Hodes syndrome | (Orphanet:3404) |
VISCERAL STEATOSIS, CONGENITAL | (OMIM:228100) |
X-linked immunoneurologic disorder | (Orphanet:2571) |