Death
Symptom Information:
| Symptom ID: | HPO:0011420 | ||
| Synonyms: |
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| Quality: | |||
| Cross references: |
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| Is a (Direct Parents): |
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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) Death(HPO:0011420) |
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| Database Frequency: | 184 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| 22q11.2 deletion syndrome | (Orphanet:567) |
| 3-hydroxyisobutyric aciduria | (Orphanet:939) |
| 46,XX disorder of sex development - anorectal anomalies | (Orphanet:2973) |
| Acalvaria | (Orphanet:945) |
| Achalasia - microcephaly | (Orphanet:929) |
| Achondrogenesis type 1A | (Orphanet:93299) |
| Achondrogenesis type 1B | (Orphanet:93298) |
| Achondrogenesis type 2 | (Orphanet:93296) |
| Acro-cardio-facial syndrome | (Orphanet:2008) |
| Acro-renal-mandibular syndrome | (Orphanet:958) |
| Acrocephalosyndactyly | (Orphanet:946) |
| Acrocraniofacial dysostosis | (Orphanet:949) |
| Acrofacial dysostosis, Rodriguez type | (Orphanet:1788) |
| Acromesomelic dysplasia, Grebe type | (Orphanet:2098) |
| Agnathia - holoprosencephaly - situs inversus | (Orphanet:990) |
| Aminopterin/methotrexate embryofetopathy | (Orphanet:1908) |
| Aniridia - ptosis - intellectual deficit - familial obesity | (Orphanet:1067) |
| Arthrogryposis - hyperkeratosis, lethal form | (Orphanet:1485) |
| Arthrogryposis multiplex congenita - whistling face | (Orphanet:1150) |
| Astley-Kendall dysplasia | (Orphanet:85175) |
| Autosomal recessive amelia | (Orphanet:1027) |
| Autosomal recessive polycystic kidney disease | (Orphanet:731) |
| Autosomal recessive spondylocostal dysostosis | (Orphanet:2311) |
| Beemer-Ertbruggen syndrome | (Orphanet:1237) |
| Bilateral renal agenesis | (Orphanet:1848) |
| Bone dysplasia, lethal Holmgren type | (Orphanet:1842) |
| Boomerang dysplasia | (Orphanet:1263) |
| Campomelia, Cumming type | (Orphanet:1318) |
| Campomelic dysplasia | (Orphanet:140) |
| Cantrell pentalogy | (Orphanet:1335) |
| Cartilage-hair hypoplasia | (Orphanet:175) |
| Caudal regression sequence | (Orphanet:3027) |
| Chondrodysplasia, Blomstrand type | (Orphanet:50945) |
| Classic galactosemia | (Orphanet:79239) |
| Cloverleaf skull - multiple congenital anomalies | (Orphanet:93267) |
| Congenital alveolar capillary dysplasia | (Orphanet:210122) |
| Congenital herpes virus infection | (Orphanet:293) |
| Congenital laryngeal web | (Orphanet:2374) |
| Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
| Congenital short bowel syndrome | (Orphanet:2301) |
| Crane-Heise syndrome | (Orphanet:1512) |
| Craniomicromelic syndrome | (Orphanet:1524) |
| Craniosynostosis - fibular aplasia | (Orphanet:1533) |
| Craniosynostosis, Herrmann-Opitz type | (Orphanet:2145) |
| Crigler-Najjar syndrome | (Orphanet:205) |
| Currarino triad | (Orphanet:1552) |
| Desmosterolosis | (Orphanet:35107) |
| Diaphanospondylodysostosis | (Orphanet:66637) |
| Diffuse neonatal hemangiomatosis | (Orphanet:2123) |
| Distal 7q11.23 microdeletion syndrome | (Orphanet:254351) |
| Distal monosomy 10p | (Orphanet:1580) |
| Distal monosomy 17q | (Orphanet:1597) |
| Distal trisomy 15q | (Orphanet:1707) |
| Donnai-Barrow syndrome | (Orphanet:2143) |
| Dysplastic cortical hyperostosis | (Orphanet:2204) |
| Dyssegmental dysplasia, Silverman-Handmaker type | (Orphanet:1865) |
| Ellis Van Creveld syndrome | (Orphanet:289) |
| Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
| Eye defects - arachnodactyly - cardiopathy | (Orphanet:2725) |
| Familial caudal dysgenesis | (Orphanet:1768) |
| Familial primary pulmonary hypoplasia | (Orphanet:2257) |
| Familial visceral myopathy | (Orphanet:2604) |
| Fanconi anemia | (Orphanet:84) |
| Fetal Gaucher disease | (Orphanet:85212) |
| Fetal akinesia deformation sequence | (Orphanet:994) |
| Fetal alcohol syndrome | (Orphanet:1915) |
| Fibrochondrogenesis | (Orphanet:2021) |
| Fibulo-ulnar hypoplasia - renal anomalies | (Orphanet:2256) |
| Fraser syndrome | (Orphanet:2052) |
| Fryns syndrome | (Orphanet:2059) |
| Galactosemia | (Orphanet:352) |
| Genito-palato-cardiac syndrome | (Orphanet:2075) |
| Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
| Hb Bart's hydrops fetalis | (Orphanet:163596) |
| Heart defects - limb shortening | (Orphanet:1354) |
| Hirschsprung disease - nail hypoplasia - dysmorphism | (Orphanet:2153) |
| Holoprosencephaly | (Orphanet:2162) |
| Holoprosencephaly - caudal dysgenesis | (Orphanet:2165) |
| Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
| Hydrolethalus | (Orphanet:2189) |
| Hypoglossia - hypodactyly | (Orphanet:989) |
| Hypomandibular faciocranial dysostosis | (Orphanet:1790) |
| Hypophosphatasia | (Orphanet:436) |
| Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit | (Orphanet:2269) |
| Indomethacin embryofetopathy | (Orphanet:1909) |
| Infantile symmetrical thalamic degeneration | (Orphanet:3311) |
| Iniencephaly | (Orphanet:63259) |
| Intellectual deficit - myopathy - short stature - endocrine defect | (Orphanet:3068) |
| Isolated anencephaly/exencephaly | (Orphanet:1048) |
| Isolated cloverleaf skull syndrome | (Orphanet:2343) |
| Isovaleric acidemia | (Orphanet:33) |
| Jeune syndrome | (Orphanet:474) |
| Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
| Laryngeal abductor paralysis | (Orphanet:2808) |
| Laryngeal abductor paralysis - intellectual deficit | (Orphanet:2375) |
| Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia | (Orphanet:2005) |
| Lethal Kniest-like dysplasia | (Orphanet:2347) |
| Lethal Larsen-like syndrome | (Orphanet:2371) |
| Lethal chondrodysplasia, Moerman type | (Orphanet:1420) |
| Lethal congenital contracture syndrome type 1 | (Orphanet:1486) |
| Lethal faciocardiomelic dysplasia | (Orphanet:1972) |
| Lethal hemolytic anemia - genital anomalies | (Orphanet:1046) |
| Lethal omphalocele-cleft palate syndrome | (Orphanet:2736) |
| Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
| Lethal recessive chondrodysplasia | (Orphanet:1423) |
| Lethal restrictive dermopathy | (Orphanet:1662) |
| Limb body wall complex | (Orphanet:2369) |
| Lower limb deficiency - hypospadias | (Orphanet:2487) |
| Macrosomia - microphthalmia - cleft palate | (Orphanet:2432) |
| Marshall-Smith syndrome | (Orphanet:561) |
| Matthew-Wood syndrome | (Orphanet:2470) |
| Meacham syndrome | (Orphanet:3097) |
| Meckel syndrome | (Orphanet:564) |
| Mesomelic dwarfism - cleft palate - camptodactyly | (Orphanet:2631) |
| Microphthalmia - microtia - fetal akinesia | (Orphanet:2547) |
| Microvillous inclusion disease | (Orphanet:2290) |
| Morse-Rawnsley-Sargent syndrome | (Orphanet:2570) |
| Mosaic trisomy 9 | (Orphanet:99776) |
| Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
| Multiple intestinal atresia | (Orphanet:2300) |
| Neu-Laxova syndrome | (Orphanet:2671) |
| Non-rhizomelic chondrodysplasia punctata | (Orphanet:176) |
| Okamoto syndrome | (Orphanet:2729) |
| Omphalocele | (Orphanet:660) |
| Ondine syndrome | (Orphanet:661) |
| Orofaciodigital syndrome type 1 | (Orphanet:2750) |
| Orofaciodigital syndrome type 2 | (Orphanet:2751) |
| Orofaciodigital syndrome type 4 | (Orphanet:2753) |
| Orofaciodigital syndrome type 5 | (Orphanet:2919) |
| Osteocraniostenosis | (Orphanet:2763) |
| Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
| Osteogenesis imperfecta | (Orphanet:666) |
| Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
| Otopalatodigital syndrome | (Orphanet:669) |
| PAGOD syndrome | (Orphanet:991) |
| Pacman dysplasia | (Orphanet:1952) |
| Pallister-Hall syndrome | (Orphanet:672) |
| Platyspondylic dysplasia, Torrance type | (Orphanet:85166) |
| Polysyndactyly - cardiac malformation | (Orphanet:2934) |
| Pontocerebellar hypoplasia type 1 | (Orphanet:2254) |
| Proximal spinal muscular atrophy | (Orphanet:70) |
| Prune belly syndrome | (Orphanet:2970) |
| Pulmonary atresia - intact ventricular septum | (Orphanet:1208) |
| Pyknoachondrogenesis | (Orphanet:3003) |
| Radio-renal syndrome | (Orphanet:3015) |
| Renal tubular dysgenesis | (Orphanet:3033) |
| Ring chromosome 10 | (Orphanet:1438) |
| Roberts syndrome | (Orphanet:3103) |
| Schinzel-Giedion syndrome | (Orphanet:798) |
| Schneckenbecken dysplasia | (Orphanet:3144) |
| Short rib-polydactyly syndrome | (Orphanet:1505) |
| Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
| Smith-Lemli-Opitz syndrome | (Orphanet:818) |
| Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
| Split hand - urinary anomalies - spina bifida | (Orphanet:2437) |
| Symmetrical thalamic calcifications | (Orphanet:1314) |
| Tetraamelia - multiple malformations | (Orphanet:3301) |
| Tetraploidy | (Orphanet:3305) |
| Thalidomide embryopathy | (Orphanet:3312) |
| Thanatophoric dysplasia | (Orphanet:2655) |
| Thanatophoric dysplasia type 1 | (Orphanet:1860) |
| Thanatophoric dysplasia type 2 | (Orphanet:93274) |
| Thin ribs - tubular bones - dysmorphism | (Orphanet:1506) |
| Thoraco-abdominal enteric duplication | (Orphanet:1759) |
| Thymic-renal-anal-lung dysplasia | (Orphanet:3326) |
| Tibial aplasia - ectrodactyly | (Orphanet:3329) |
| Toriello-Carey syndrome | (Orphanet:3338) |
| Tracheal agenesis | (Orphanet:3346) |
| Tracheo-esophageal fistula - hypospadias | (Orphanet:2042) |
| Triose phosphate-isomerase deficiency | (Orphanet:868) |
| Triploidy | (Orphanet:3376) |
| Trisomy 13 | (Orphanet:3378) |
| Trisomy 18 | (Orphanet:3380) |
| Trisomy 1q | (Orphanet:261344) |
| Uhl anomaly | (Orphanet:3403) |
| Ulbright-Hodes syndrome | (Orphanet:3404) |
| VACTERL with hydrocephalus | (Orphanet:3412) |
| VACTERL/VATER association | (Orphanet:887) |
| Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
| Wolf-Hirschhorn syndrome | (Orphanet:280) |
| X-linked centronuclear myopathy | (Orphanet:596) |
| X-linked immunoneurologic disorder | (Orphanet:2571) |
| XK aprosencephaly | (Orphanet:3469) |
| Yunis-Varon syndrome | (Orphanet:3472) |