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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   hydatidiform mole
  

Disease ID 422
Disease hydatidiform mole
Definition
Trophoblastic hyperplasia associated with normal gestation, or molar pregnancy. It is characterized by the swelling of the CHORIONIC VILLI and elevated human CHORIONIC GONADOTROPIN. Hydatidiform moles or molar pregnancy may be categorized as complete or partial based on their gross morphology, histopathology, and karyotype.
Synonym
[m]hydatidiform mole nos
[m]hydatidiform mole nos (morphologic abnormality)
chorionic tumor
classical hydatidiform mole
gestational trophoblastic tumor, hydatidiform mole
gtt, hydatidiform mole
hydatid mole
hydatid moles
hydatidiform mole (disorder)
hydatidiform mole (morphologic abnormality)
hydatidiform mole [ambiguous]
hydatidiform mole [disease/finding]
hydatidiform mole gtt
hydatidiform mole, no icd-o subtype
hydatidiform mole, no icd-o subtype (morphologic abnormality)
hydatidiform mole, no international classification of diseases for oncology subtype
hydatidiform mole, no international classification of diseases for oncology subtype (morphologic abnormality)
hydatidiform mole, nos
hydatidiform moles
molar pregn
molar pregnancies
molar pregnancy
molar pregnancy (disorder)
molar pregnancy with hydatid mole
molar pregnancy with hydatidiform mole
molar pregnancy with hydatidiform mole (disorder)
molar pregnancy with hydatidiform mole (disorder) [ambiguous]
molar pregnancy with vesicular mole
molar pregnancy with vesicular mole (disorder)
molar pregnancy, nos
molars pregnancy
mole
mole (disorder)
mole -retired-
mole hydatidiform
mole of pregnancy
mole of pregnancy, nos
mole pregnancy
mole, hydatid
mole, hydatidiform
mole, nos
moles pregnancy
moles, hydatid
moles, hydatidiform
pregn molar
pregnancies, molar
pregnancy mole
pregnancy, molar
vesicular mole
Orphanet
OMIM
DOID
ICD10
UMLS
C0020217
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:30)
C0008497  |  choriocarcinoma  |  4
C0020550  |  hyperthyroidism  |  3
C0032987  |  ectopic pregnancy  |  3
C0025202  |  melanoma  |  2
C1135868  |  gestational trophoblastic disease  |  2
C0019343  |  pemphigoid gestationis  |  2
C0085083  |  ovarian hyperstimulation syndrome  |  2
C0152095  |  trisomy 13  |  1
C0027706  |  hereditary nephritis  |  1
C0022658  |  nephropathy  |  1
C0013537  |  eclampsia  |  1
C0019114  |  hemosiderosis  |  1
C0018802  |  congestive heart failure  |  1
C0027726  |  nephrotic syndrome  |  1
C0022408  |  arthropathy  |  1
C0017105  |  gas gangrene  |  1
C0027697  |  nephritis  |  1
C0040127  |  thyroid storm  |  1
C0020538  |  hypertension  |  1
C0677608  |  chorioangioma  |  1
C0018801  |  heart failure  |  1
C0034150  |  purpura  |  1
C0034155  |  thrombotic thrombocytopenic purpura  |  1
C0030805  |  pemphigoid  |  1
C0878544  |  cardiomyopathy  |  1
C0745140  |  hyperthyroid  |  1
C0003857  |  arteriovenous malformation  |  1
C1135868  |  gestational trophoblastic neoplasia  |  1
C0040053  |  thrombus  |  1
C0032914  |  preeclampsia  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
199713  |  NLRP7  |  CTD_human;UNIPROT
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 422
Disease hydatidiform mole
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:8)
HP:0005268  |  Spontaneous abortion
HP:0000119  |  Genitourinary abnormality
HP:0100602  |  Preeclampsia
HP:0100878  |  Enlarged uterus
HP:0400008  |  Menometrorrhagia
HP:0002017  |  Nausea and vomiting
HP:0001903  |  Anemia
HP:0000836  |  Hyperthyroidism
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:25)
HP:0100768  |  Choriocarcinoma  |  4
HP:0000836  |  Overactive thyroid  |  3
HP:0002861  |  Melanoma  |  2
HP:0003764  |  Naevus  |  2
HP:0000123  |  Nephritis  |  1
HP:0012721  |  Venous malformations  |  1
HP:0100601  |  Eclampsia  |  1
HP:0001945  |  Fever  |  1
HP:0200058  |  Angiosarcoma  |  1
HP:0000112  |  Nephropathy  |  1
HP:0002664  |  Neoplasia  |  1
HP:0000100  |  Nephrosis  |  1
HP:0012531  |  Pain  |  1
HP:0002315  |  Headaches  |  1
HP:0006267  |  Placental enlargement  |  1
HP:0012378  |  Fatigue  |  1
HP:0001635  |  Congestive heart failure  |  1
HP:0003040  |  Arthropathy  |  1
HP:0001000  |  Pigmentary changes  |  1
HP:0100749  |  Thoracic pain  |  1
HP:0000822  |  Hypertension  |  1
HP:0000979  |  Purpura  |  1
HP:0001638  |  Cardiomyopathy  |  1
HP:0100026  |  Arteriovenous malformation  |  1
HP:0100602  |  Pre-eclampsia  |  1
Disease ID 422
Disease hydatidiform mole
Manually Symptom
UMLS  | Name(Total Manually Symptoms:13)
C1608408  |  malignant transformation
C1135868  |  trophoblastic disease
C1135868  |  gestational trophoblastic disease
C1000483  |  anemia
C0553681  |  hypofibrinogenemia
C0040156  |  thyrotoxicosis
C0034065  |  pulmonary embolism
C0034063  |  pulmonary edema
C0032914  |  pre-eclampsia
C0030584  |  parovarian cyst
C0020550  |  hyperthyroidism
C0013537  |  eclampsia
C0000727  |  acute abdomen
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:5)
C1135868  |  trophoblastic disease  |  2
C0020550  |  hyperthyroidism  |  2
C0032914  |  preeclampsia  |  1
C1608408  |  malignant transformation  |  1
C0013537  |  eclampsia  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:2)
HP ID HP Name MP ID MP Name Annotation
HP:0000119Abnormality of the genitourinary systemMP:0004251failure of heart loopingfailure of the primitive heart tube to loop asymmetrically during early development
HP:0002017Nausea and vomitingMP:0010426abnormal heart and great artery attachmentany anomaly in the in the position or pattern of the connection site of the heart to any of the great arteries, including the pulmonary artery and aorta
Mapped by homologous gene(Total Items:6)
HP ID HP Name MP ID MP Name Annotation
HP:0000836HyperthyroidismMP:0020169increased thyroid gland weighthigher than average weight of the thyroid gland
HP:0005268Spontaneous abortionMP:0020040decreased bone ossificationdecrease in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance
HP:0002017Nausea and vomitingMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0100602PreeclampsiaMP:0014169decreased brown adipose tissue massdecreased physical bulk or volume of brown adipose tissue
HP:0001903AnemiaMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0000119Abnormality of the genitourinary systemMP:0013348adenohypophysis hyperplasia overdevelopment or increased size of the anterior lobe of the pituitary gland, usually due to increased cell number
Disease ID 422
Disease hydatidiform mole
Case(Waiting for update.)