Maternal diabetes

Symptom Information:

Symptom ID: HPO:0009800
Synonyms:
gestational diabetes [HPO:0009800]
maternal hyperglycemia [HPO:0009800]
Gestational diabetes mellitus (disorder) [Orphanet:55600]
Gestational Diabetes [Orphanet:55600]
Gestational diabetes [OMIM:Gestational diabetes]
Maternal diabetes [Orphanet:55600]
Gestational diabetes [Orphanet:55600]
Gestational diabetes [MedDRA:10018209]
Diabetes in pregnancy [MedDRA:10018209]
Diabetes mellitus gestational [MedDRA:10018209]
Diabetes mellitus, antepartum [MedDRA:10018209]
Diabetes mellitus, postpartum [MedDRA:10018209]
Gestational diabetes mellitus [MedDRA:10018209]
Quality:
Cross references:
Orphanet:55600 "Maternal diabetes" [Orphanet:55600]
OMIM: "Gestational diabetes" [OMIM:Gestational diabetes]
UMLS:C0085207 "Gestational Diabetes" [Orphanet:55600]
Is a (Direct Parents):
Orphanet Abnormality of prenatal development or birth
MedDRA Pregnancy complicated by maternal disorders
HPO         Diabetes mellitus
HPO         Prenatal maternal abnormality
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)