Large for gestational age

Symptom Information:

Symptom ID: HPO:0001520
Synonyms:
Birth weight > 90th percentile [HPO:0001520]
Birthweight > 90th percentile [HPO:0001520]
Fetal macrosomia [HPO:0001520]
Macrosomia [HPO:0001520]
Macrosomia, neonatal [HPO:0001520]
Birth weight > 90th percentile [OMIM:Birth weight > 90th percentile]
Birthweight > 90th percentile [OMIM:Birthweight > 90th percentile]
Large for gestational age [OMIM:Large for gestational age]
Macrosomia [OMIM:Macrosomia]
Macrosomia, neonatal [OMIM:Macrosomia, neonatal]
Birth weight >90th percentile [OMIM:Birth weight >90th percentile]
Macrosomia (1 patient) [OMIM:Macrosomia (1 patient)]
Macrosomia [MedDRA:10025394]
Quality:
Cross references:
OMIM: "Birth weight > 90th percentile" [OMIM:Birth weight > 90th percentile]
OMIM: "Birthweight > 90th percentile" [OMIM:Birthweight > 90th percentile]
OMIM: "Large for gestational age" [OMIM:Large for gestational age]
OMIM: "Macrosomia" [OMIM:Macrosomia]
OMIM: "Macrosomia, neonatal" [OMIM:Macrosomia, neonatal]
OMIM: "Birth weight >90th percentile" [OMIM:Birth weight >90th percentile]
OMIM: "Macrosomia (1 patient)" [OMIM:Macrosomia (1 patient)]
Is a (Direct Parents):
HPO         Increased body weight
MedDRA General signs and symptoms NEC
HPO         Overgrowth
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Growth abnormality(HPO:0001507)
          Abnormality of body weight(HPO:0004323)
             Increased body weight(HPO:0004324)
                Large for gestational age(HPO:0001520)
          Overgrowth(HPO:0001548)
             Large for gestational age(HPO:0001520)
MedDRA:
General disorders and administration site conditions(MedDRA:10018065)
    General system disorders NEC(MedDRA:10018073)
       General signs and symptoms NEC(MedDRA:10018072)
          Large for gestational age(HPO:0001520)
Database Frequency: 34 / 7739
Resource:

All diseases associated with this symptom:

ABCD SYNDROME (OMIM:600501)
Acromegaloid facial appearance syndrome (Orphanet:965)
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency (Orphanet:276580)
Autosomal dominant hyperinsulinism due to SUR1 deficiency (Orphanet:276575)
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency (Orphanet:79644)
Autosomal recessive hyperinsulinism due to SUR1 deficiency (Orphanet:79643)
Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
Beckwith-Wiedemann syndrome due to 11p15 microduplication (Orphanet:96076)
Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion (Orphanet:231130)
Beckwith-Wiedemann syndrome due to CDKN1C mutation (Orphanet:231120)
Beckwith-Wiedemann syndrome due to NSD1 mutation (Orphanet:238613)
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 (Orphanet:231117)
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 (Orphanet:96193)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Cleft lip/palate - intestinal malrotation - cardiopathy (Orphanet:2001)
Costello syndrome (Orphanet:3071)
Diabetic embryopathy (Orphanet:1926)
Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency (Orphanet:276603)
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency (Orphanet:276598)
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY (OMIM:614520)
FACIOCARDIOMELIC SYNDROME (OMIM:612731)
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THEYOUNG (OMIM:616026)
Fryns syndrome (Orphanet:2059)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypoinsulinemic hypoglycemia and body hemihypertrophy (Orphanet:293964)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
MACROSOMIA ADIPOSA CONGENITA (OMIM:248100)
MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES (OMIM:606772)
Macrosomia - microphthalmia - cleft palate (Orphanet:2432)
Maturity-onset diabetes of the young, type 1 (OMIM:125850)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
Perlman syndrome (Orphanet:2849)
Zunich-Kaye syndrome (Orphanet:3474)