Neonatal hypoglycemia
Symptom Information:
Symptom ID: | HPO:0001998 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) |