Maternal diabetes
Symptom Information:
Symptom ID: | HPO:0009800 | |||||||||||||
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) Diabetes mellitus(HPO:0000819) Maternal diabetes(HPO:0009800) Abnormality of the endocrine system(HPO:0000818) Diabetes mellitus(HPO:0000819) Maternal diabetes(HPO:0009800) Abnormality of prenatal development or birth(HPO:0001197) Prenatal maternal abnormality(HPO:0002686) Maternal diabetes(HPO:0009800) MedDRA: Pregnancy, puerperium and perinatal conditions(MedDRA:10036585) Maternal complications of pregnancy(MedDRA:10026908) Pregnancy complicated by maternal disorders(MedDRA:10052745) Maternal diabetes(HPO:0009800) |
|||||||||||||
Database Frequency: | 14 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
Caudal regression sequence | (Orphanet:3027) |
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Femoral-facial syndrome | (Orphanet:1988) |
Foix-Chavany-Marie syndrome | (Orphanet:2048) |
Hypoplastic left heart syndrome | (Orphanet:2248) |
Neurogenic arthrogryposis multiplex congenita | (Orphanet:1143) |
Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
Partial pancreatic agenesis | (Orphanet:2805) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Sacrococcygeal dysgenesis association | (Orphanet:1773) |
Septo-optic dysplasia | (Orphanet:3157) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
Symbrachydactyly of hands and feet | (Orphanet:1570) |
Ulbright-Hodes syndrome | (Orphanet:3404) |