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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Pregnancy Complications (D011248)
..Starting node ..Oligohydramnios (D016104)
Child Nodes:
........Urethral obstruction sequence (C536477)
Sister Nodes:
..Abortion, Spontaneous (D000022) 9
..Acute fatty liver of pregnancy (C537957)
..Chorea Gravidarum (D020150)
..Diabetes, Gestational (D016640) 5
..Fetal Death (D005313) 4
..Fetal Diseases (D005315) 51
..Hypertension, Pregnancy-Induced (D046110) 7
..Hyperthyroidism, Familial Gestational (C566384)
..Intrahepatic Cholestasis of Pregnancy (C535932)
..Maternal Death (D063130)
..Morning Sickness (D048968) 1
..Nuchal Cord (D053589)
..Obstetric Labor Complications (D007744) 17
..Oligohydramnios (D016104) 1
..Pelvic Floor Disorders (D059952)
..Pemphigoid Gestationis (D006559)
..Perinatal Death (D066087)
..Phenylketonuria, Maternal (D017042)
..Placenta Diseases (D010922) 6
..Polyhydramnios (D006831) 4
..Pregnancy Complications, Cardiovascular (D011249) 1
..Pregnancy Complications, Hematologic (D011250)
..Pregnancy Complications, Infectious (D011251) 4
..Pregnancy Complications, Neoplastic (D011252) 7
..Pregnancy in Diabetics (D011254) 6
..Pregnancy, Ectopic (D011271) 7
..Pregnancy, Prolonged (D011273)
..Prenatal Injuries (D049188) 1
..Pruritic urticarial papules plaques of pregnancy (C535817)
..Puerperal Disorders (D011644) 13
..Twinning due to Superfetation (C566018)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8218
Name:	Oligohydramnios
Definition:	A condition of abnormally low AMNIOTIC FLUID volume. Principal causes include malformations of fetal URINARY TRACT; FETAL GROWTH RETARDATION; GESTATIONAL HYPERTENSION; nicotine poisoning; and PROLONGED PREGNANCY.
Alternative IDs:
ParentIDs:	MESH:D011248
TreeNumbers:	C13.703.560
Synonyms:
Slim Mappings:	Pregnancy complication
Reference:	MedGen: D016104 MeSH: D016104 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants