Premature birth

Symptom Information:

Symptom ID: HPO:0001622
Synonyms:
Premature delivery [HPO:0001622]
Premature delivery of affected infants [HPO:0001622]
Preterm delivery [HPO:0001622]
Premature pregnancy delivered (finding) [Orphanet:55120]
Premature delivery (finding) [Orphanet:55120]
Prematurity of fetus (disorder) [Orphanet:55120]
Prematurity of fetus [Orphanet:55120]
Premature Birth [Orphanet:55120]
Premature birth [OMIM:Premature birth]
Premature delivery [OMIM:Premature delivery]
Premature delivery of affected infants [OMIM:Premature delivery of affected infants]
Preterm delivery [OMIM:Preterm delivery]
Prematurity [Orphanet:55120]
Premature delivery [Orphanet:55120]
Premature baby [MedDRA:10036590]
Baby 28 weeks plus under 2.5 kg [MedDRA:10036590]
Baby premature [MedDRA:10036590]
Birth premature [MedDRA:10036590]
Extreme immaturity [MedDRA:10036590]
Extreme immaturity, 1,000-1,249 grams [MedDRA:10036590]
Extreme immaturity, 1,250-1,499 grams [MedDRA:10036590]
Extreme immaturity, 1,500-1,749 grams [MedDRA:10036590]
Extreme immaturity, 1,750-1,999 grams [MedDRA:10036590]
Extreme immaturity, 2,000-2,499 grams [MedDRA:10036590]
Extreme immaturity, 2,500+ grams [MedDRA:10036590]
Extreme immaturity, 500-749 grams [MedDRA:10036590]
Extreme immaturity, 750-999 grams [MedDRA:10036590]
Extreme immaturity, less than 500 grams [MedDRA:10036590]
Extreme immaturity, unspecified {weight} [MedDRA:10036590]
Immature baby [MedDRA:10036590]
Infant premature [MedDRA:10036590]
Other preterm infants [MedDRA:10036590]
Other preterm infants, 1,000-1,249 grams [MedDRA:10036590]
Other preterm infants, 1,250-1,499 grams [MedDRA:10036590]
Other preterm infants, 1,500-1,749 grams [MedDRA:10036590]
Other preterm infants, 1,750-1,999 grams [MedDRA:10036590]
Other preterm infants, 2,000-2,499 grams [MedDRA:10036590]
Other preterm infants, 2,500+ grams [MedDRA:10036590]
Other preterm infants, 500-749 grams [MedDRA:10036590]
Other preterm infants, 750-999 grams [MedDRA:10036590]
Other preterm infants, less than 500 grams [MedDRA:10036590]
Other preterm infants, unspecified {weight} [MedDRA:10036590]
Premature birth [MedDRA:10036590]
Prematurity [MedDRA:10036590]
Prematurity syndrome [MedDRA:10036590]
Syndrome prematurity [MedDRA:10036590]
Premature baby 26 to 32 weeks [MedDRA:10036590]
Premature baby 33 to 36 weeks [MedDRA:10036590]
Premature baby less than 26 weeks [MedDRA:10036590]
Premature delivery [MedDRA:10036595]
Early onset of delivery [MedDRA:10036595]
Early onset of delivery, delivered, with or without mention of antepartum condition [MedDRA:10036595]
Early onset of delivery, unspecified as to episode of care [MedDRA:10036595]
Prematurity [OMIM:Prematurity]
Quality:
Cross references:
Orphanet:55120 "Prematurity" [Orphanet:55120]
OMIM: "Premature birth" [OMIM:Premature birth]
OMIM: "Premature delivery" [OMIM:Premature delivery]
OMIM: "Premature delivery of affected infants" [OMIM:Premature delivery of affected infants]
OMIM: "Preterm delivery" [OMIM:Preterm delivery]
OMIM: "Prematurity" [OMIM:Prematurity]
UMLS:C0728731 "Prematurity of fetus" [Orphanet:55120]
UMLS:C0151526 "Premature Birth" [Orphanet:55120]
Is a (Direct Parents):
MedDRA Labour onset and length abnormalities
Orphanet Abnormality of prenatal development or birth
MedDRA Gestational age and weight conditions
HPO         Abnormality of prenatal development or birth
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of prenatal development or birth(HPO:0001197)
          Premature birth(HPO:0001622)
MedDRA:
Pregnancy, puerperium and perinatal conditions(MedDRA:10036585)
    Neonatal and perinatal conditions(MedDRA:10028920)
       Gestational age and weight conditions(MedDRA:10018208)
          Premature birth(HPO:0001622)
    Maternal complications of labour and delivery(MedDRA:10026906)
       Labour onset and length abnormalities(MedDRA:10000192)
          Premature birth(HPO:0001622)
Database Frequency: 100 / 7739
Resource:

All diseases associated with this symptom:

AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA (OMIM:613623)
Acrofacial dysostosis, Catania type (Orphanet:1786)
Adams-Oliver syndrome (Orphanet:974)
Atelosteogenesis type I (Orphanet:1190)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
BARTTER SYNDROME, ANTENATAL, TYPE 1 (OMIM:601678)
BARTTER SYNDROME, TYPE 4B (OMIM:613090)
Bartter syndrome (Orphanet:112)
Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
Beckwith-Wiedemann syndrome due to CDKN1C mutation (Orphanet:231120)
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 (Orphanet:231117)
Blackfan-Diamond anemia (Orphanet:124)
CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3 (OMIM:614972)
CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1 (OMIM:147480)
CINCA syndrome (Orphanet:1451)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Caudal appendage - deafness (Orphanet:1123)
Chondrodysplasia, Blomstrand type (Orphanet:50945)
Congenital chloride diarrhea (Orphanet:53689)
Congenital herpes virus infection (Orphanet:293)
Congenital lethal myopathy, Compton-North type (Orphanet:210163)
Congenital pulmonary airway malformation (Orphanet:2444)
Congenital toxoplasmosis (Orphanet:858)
Cornelia de Lange syndrome (Orphanet:199)
Costello syndrome (Orphanet:3071)
DIAMOND-BLACKFAN ANEMIA 1 (OMIM:105650)
Diffuse neonatal hemangiomatosis (Orphanet:2123)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal monosomy 17q (Orphanet:1597)
Dysmorphism - conductive hearing loss - heart defect (Orphanet:289553)
Ebstein malformation (Orphanet:1880)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Epidermolysis bullosa simplex with pyloric atresia (Orphanet:158684)
Familial hyperthyroidism due to mutations in TSH receptor (Orphanet:424)
Fetal Gaucher disease (Orphanet:85212)
Fetal akinesia deformation sequence (Orphanet:994)
Fibular aplasia - ectrodactyly (Orphanet:1118)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
Fowler syndrome (Orphanet:221126)
Free sialic acid storage disease, infantile form (Orphanet:309324)
GMS syndrome (Orphanet:2090)
Galloway-Mowat syndrome (Orphanet:2065)
HEC syndrome (Orphanet:2119)
Harlequin ichthyosis (Orphanet:457)
Holoprosencephaly - caudal dysgenesis (Orphanet:2165)
Hydrolethalus (Orphanet:2189)
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome (Orphanet:363694)
Ichthyosis prematurity syndrome (Orphanet:88621)
Imperforate oropharynx - costo vetebral anomalies (Orphanet:2759)
Indomethacin embryofetopathy (Orphanet:1909)
Infant acute respiratory distress syndrome (Orphanet:70587)
Infantile Bartter syndrome with deafness (Orphanet:89938)
Intrahepatic cholestasis of pregnancy (Orphanet:69665)
Jacobsen syndrome (Orphanet:2308)
KAGAMI-OGATA SYNDROME (OMIM:608149)
Lethal Kniest-like dysplasia (Orphanet:2347)
Lethal infantile mitochondrial myopathy (Orphanet:254857)
Lethal restrictive dermopathy (Orphanet:1662)
Limb transversal defect - cardiac anomaly (Orphanet:2492)
Lower limb deficiency - hypospadias (Orphanet:2487)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
NEMALINE MYOPATHY 10 (OMIM:616165)
Nager syndrome (Orphanet:245)
Neonatal hemochromatosis (Orphanet:446)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
OSTEOGENESIS IMPERFECTA, TYPE II (OMIM:166210)
Omphalocele (Orphanet:660)
Osteogenesis imperfecta type 2 (Orphanet:216804)
POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY (OMIM:611087)
Pachygyria - intellectual deficit - epilepsy (Orphanet:2798)
Patent arterial duct (Orphanet:706)
Pelizaeus-Merzbacher disease (Orphanet:702)
Pelizaeus-Merzbacher-like disease (Orphanet:280270)
Pemphigoid gestationis (Orphanet:63275)
Ptosis - vocal cord paralysis (Orphanet:2997)
Pyknoachondrogenesis (Orphanet:3003)
Pyridoxal phosphate-responsive seizures (Orphanet:79096)
Renal tubular dysgenesis (Orphanet:3033)
Reticular dysgenesis (Orphanet:33355)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)
Roberts syndrome (Orphanet:3103)
Roifman syndrome (Orphanet:353298)
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 (OMIM:604320)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Spinal muscular atrophy with respiratory distress (Orphanet:98920)
Splenogonadal fusion - limb defects - micrognathia (Orphanet:2063)
Stern-Lubinsky-Durrie syndrome (Orphanet:3194)
Synostosis - microcephaly - scoliosis (Orphanet:3268)
TEMPLE SYNDROME (OMIM:616222)
VACTERL with hydrocephalus (Orphanet:3412)
VACTERL/VATER association (Orphanet:887)
VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE (OMIM:219730)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Velo-facial-skeletal syndrome (Orphanet:3424)
Yunis-Varon syndrome (Orphanet:3472)
Zellweger syndrome (Orphanet:912)