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PedAM

Pediatric Disease Annotations & Medicines



   cavernous hemangioma
  

Disease ID 1757
Disease cavernous hemangioma
Definition
A vascular anomaly that is a collection of tortuous BLOOD VESSELS and connective tissue. This tumor-like mass with the large vascular space is filled with blood and usually appears as a strawberry-like lesion in the subcutaneous areas of the face, extremities, or other regions of the body including the central nervous system.
Synonym
[m]cavernous haemangioma
[m]cavernous hemangioma
cavernoma
cavernous angioma
cavernous angioma of skin
cavernous haemangioma
cavernous haemangioma (disorder)
cavernous hemangioma (disorder)
cavernous hemangioma (morphologic abnormality)
cavernous hemangiomas
cavernous naevus
cavernous naevus of skin
cavernous nevus
cavernous nevus of skin
hemangioma cavernous
hemangioma, cavernous
hemangioma, cavernous [disease/finding]
hemangioma, mature
hemangioma, strawberry
hemangiomas, cavernous
hemangiomas, strawberry
strawberry haemangioma
strawberry haemangioma (disorder)
strawberry hemangioma
strawberry hemangiomas
DOID
UMLS
C0018920
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:19)
C0238246  |  hepatic hemangioma  |  4
C0040053  |  thrombosis  |  3
C0018916  |  hemangioma  |  3
C0040053  |  thrombus  |  2
C0002871  |  anemia  |  1
C0022350  |  dubin-johnson syndrome  |  1
C0035335  |  retinoblastoma  |  1
C0034150  |  peliosis  |  1
C0036439  |  scoliosis  |  1
C0040034  |  thrombocytopenia  |  1
C0238246  |  liver hemangioma  |  1
C0031039  |  pericardial effusion  |  1
C0026896  |  myasthenia gravis  |  1
C0019158  |  hepatitis  |  1
C0040046  |  thrombophlebitis  |  1
C0019163  |  hepatitis b  |  1
C0010481  |  cushing's syndrome  |  1
C0018920  |  cavernous hemangiomas  |  1
C0020541  |  portal hypertension  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:96)
10301  |  DLEU1  |  DISEASES
2519  |  FUCA2  |  DISEASES
84245  |  MRI1  |  DISEASES
3053  |  SERPIND1  |  DISEASES
7431  |  VIM  |  DISEASES
55856  |  ACOT13  |  DISEASES
5911  |  RAP2A  |  DISEASES
968  |  CD68  |  DISEASES
5908  |  RAP1B  |  DISEASES
1144  |  CHRND  |  DISEASES
3442  |  IFNA5  |  DISEASES
6386  |  SDCBP  |  DISEASES
1134  |  CHRNA1  |  DISEASES
7450  |  VWF  |  DISEASES
6558  |  SLC12A2  |  DISEASES
9368  |  SLC9A3R1  |  DISEASES
10133  |  OPTN  |  DISEASES
2033  |  EP300  |  DISEASES
3791  |  KDR  |  DISEASES
4437  |  MSH3  |  DISEASES
320  |  APBA1  |  DISEASES
2515  |  ADAM2  |  DISEASES
7157  |  TP53  |  DISEASES
6531  |  SLC6A3  |  DISEASES
2702  |  GJA5  |  DISEASES
5352  |  PLOD2  |  DISEASES
9510  |  ADAMTS1  |  DISEASES
2776  |  GNAQ  |  DISEASES
1145  |  CHRNE  |  DISEASES
7039  |  TGFA  |  DISEASES
64320  |  RNF25  |  DISEASES
213  |  ALB  |  DISEASES
719  |  C3AR1  |  DISEASES
3689  |  ITGB2  |  DISEASES
1140  |  CHRNB1  |  DISEASES
2147  |  F2  |  DISEASES
947  |  CD34  |  DISEASES
9743  |  ARHGAP32  |  DISEASES
8557  |  TCAP  |  DISEASES
713  |  C1QB  |  DISEASES
3078  |  CFHR1  |  DISEASES
3039  |  HBA1  |  DISEASES
64764  |  CREB3L2  |  DISEASES
8303  |  SNN  |  DISEASES
9939  |  RBM8A  |  DISEASES
54821  |  ERCC6L  |  DISEASES
9138  |  ARHGEF1  |  DISEASES
23583  |  SMUG1  |  DISEASES
51337  |  THEM6  |  DISEASES
1528  |  CYB5A  |  DISEASES
2701  |  GJA4  |  DISEASES
53827  |  FXYD5  |  DISEASES
889  |  KRIT1  |  DISEASES
7316  |  UBC  |  DISEASES
5906  |  RAP1A  |  DISEASES
6525  |  SMTN  |  DISEASES
23644  |  EDC4  |  DISEASES
23607  |  CD2AP  |  DISEASES
2157  |  F8  |  DISEASES
6238  |  RRBP1  |  DISEASES
58  |  ACTA1  |  DISEASES
1380  |  CR2  |  DISEASES
10877  |  CFHR4  |  DISEASES
462  |  SERPINC1  |  DISEASES
10767  |  HBS1L  |  DISEASES
4288  |  MKI67  |  DISEASES
8771  |  TNFRSF6B  |  DISEASES
5236  |  PGM1  |  DISEASES
8813  |  DPM1  |  DISEASES
7422  |  VEGFA  |  DISEASES
2517  |  FUCA1  |  DISEASES
714  |  C1QC  |  DISEASES
712  |  C1QA  |  DISEASES
177  |  AGER  |  DISEASES
53358  |  SHC3  |  DISEASES
6839  |  SUV39H1  |  DISEASES
353116  |  RILPL1  |  DISEASES
7905  |  REEP5  |  DISEASES
3440  |  IFNA2  |  DISEASES
3662  |  IRF4  |  DISEASES
83605  |  CCM2  |  DISEASES
7053  |  TGM3  |  DISEASES
192668  |  CYS1  |  DISEASES
55576  |  STAB2  |  DISEASES
2175  |  FANCA  |  DISEASES
11235  |  PDCD10  |  DISEASES
3426  |  CFI  |  DISEASES
6164  |  RPL34  |  DISEASES
174  |  AFP  |  DISEASES
57703  |  CWC22  |  DISEASES
25821  |  MTO1  |  DISEASES
6628  |  SNRPB  |  DISEASES
6513  |  SLC2A1  |  DISEASES
1379  |  CR1L  |  DISEASES
2053  |  EPHX2  |  DISEASES
7033  |  TFF3  |  DISEASES
Locus(Waiting for update.)
Disease ID 1757
Disease cavernous hemangioma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:27)
HP:0007461  |  Hemangiomatosis  |  4
HP:0001028  |  Strawberry mark  |  3
HP:0002664  |  Neoplasia  |  2
HP:0000790  |  Hematuria  |  2
HP:0004418  |  Thrombophlebitis  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0003418  |  Back pain  |  1
HP:0011896  |  Subconjunctival hemorrhage  |  1
HP:0030665  |  Holmes' tremor  |  1
HP:0002239  |  Gastrointestinal hemorrhage  |  1
HP:0012531  |  Pain  |  1
HP:0007902  |  Vitreous hemorrhage  |  1
HP:0009919  |  Retinoblastoma  |  1
HP:0002650  |  Scoliosis  |  1
HP:0002027  |  Abdominal pain  |  1
HP:0001250  |  Seizures  |  1
HP:0001337  |  Tremor  |  1
HP:0001698  |  Pericardial effusions  |  1
HP:0001907  |  Thromboembolic disease  |  1
HP:0006254  |  Increased serum alpha-fetoprotein  |  1
HP:0001873  |  Low platelet count  |  1
HP:0000073  |  Ureteral duplication  |  1
HP:0002584  |  Intestinal hemorrhage  |  1
HP:0001903  |  Anemia  |  1
HP:0012721  |  Venous malformations  |  1
HP:0001409  |  Portal hypertension  |  1
HP:0003473  |  Fatigable weakness  |  1
Disease ID 1757
Disease cavernous hemangioma
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0019080  |  hemorrhage  |  4
Manually Genotype(Total Text Mining 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:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)