Premature birth
Symptom Information:
Symptom ID: | HPO:0001622 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |