Symptom Information:

Symptom ID: HPO:0011420
Death [MedDRA:10011906]
Cross references:
Is a (Direct Parents):
MedDRA Death and sudden death
Is a (Whole tree): HPO:
General disorders and administration site conditions(MedDRA:10018065)
    Fatal outcomes(MedDRA:10053172)
       Death and sudden death(MedDRA:10011907)
Database Frequency: 184 / 7739

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)