Neonatal hypoglycemia

Symptom Information:

Symptom ID: HPO:0001998
Synonyms:
Neonatal hypoglycemia [OMIM:Neonatal hypoglycemia]
Hypoglycemia, neonatal (in some patients) [OMIM:Hypoglycemia, neonatal (in some patients)]
Quality:
Cross references:
OMIM: "Neonatal hypoglycemia" [OMIM:Neonatal hypoglycemia]
OMIM: "Hypoglycemia, neonatal (in some patients)" [OMIM:Hypoglycemia, neonatal (in some patients)]
Is a (Direct Parents):
HPO         Hypoglycemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013)
             Abnormal glucose homeostasis(HPO:0011014)
                Abnormality of blood glucose concentration(HPO:0011015)
                   Hypoglycemia(HPO:0001943)
                      Neonatal hypoglycemia(HPO:0001998)
MedDRA:
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

AICA-ribosiduria (Orphanet:250977)
Beckwith-Wiedemann syndrome (Orphanet:116)
Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
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)
Costello syndrome (Orphanet:3071)
Dopamine beta-hydroxylase deficiency (Orphanet:230)
Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease (Orphanet:439854)
Glycogen storage disease due to hepatic glycogen synthase deficiency (Orphanet:2089)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hypoinsulinemic hypoglycemia and body hemihypertrophy (Orphanet:293964)
Hypotonia - cystinuria syndrome (Orphanet:163690)
KABUKI SYNDROME 2 (OMIM:300867)
Leprechaunism (Orphanet:508)
MELAS (Orphanet:550)
PITUITARY HORMONE DEFICIENCY, COMBINED, 2 (OMIM:262600)
Panhypopituitarism (Orphanet:90695)
Septo-optic dysplasia (Orphanet:3157)
[DEL] GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL (OMIM:261740)