Large for gestational age
Symptom Information:
Symptom ID: | HPO:0001520 | |||||||||||||
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) Growth abnormality(HPO:0001507) Overgrowth(HPO:0001548) Large for gestational age(HPO:0001520) Abnormality of body weight(HPO:0004323) Increased body weight(HPO:0004324) 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) |
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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) |