PedAM

Pediatric Disease Annotations & Medicines


	capillary hemangioma

Disease ID	1404
Disease	capillary hemangioma
Definition	A dull red, firm, dome-shaped hemangioma, sharply demarcated from surrounding skin, usually located on the head and neck, which grows rapidly and generally undergoes regression and involution without scarring. It is caused by proliferation of immature capillary vessels in active stroma, and is usually present at birth or occurs within the first two or three months of life. (Dorland, 27th ed)
Synonym	angiomas strawberry angiomatous naevus angiomatous naevus of skin angiomatous nevus angiomatous nevus of skin birthmarks strawberry capillary angioma capillary haemangioma capillary haemangioma of skin capillary hemangioma (disorder) capillary hemangioma (morphologic abnormality) capillary hemangioma of skin capillary hemangiomas capillary naevus capillary naevus of skin capillary nevus capillary nevus of skin cellular hemangioma congenital vascular hamartoma congenital vascular naevus congenital vascular nevus congenital vascular nevus (disorder) haemangioma simplex hemangioma simplex hemangioma strawberry hemangioma, capillary hemangioma, capillary [disease/finding] hemangiomas infantile hemangiomas strawberry hemangiomas, capillary infantile haemangioma infantile hemangioendothelioma infantile hemangioma juvenile capillary hemangioma juvenile haemangioma juvenile hemangioma mark strawberry marks strawberry nevus capillary plexiform haemangioma plexiform hemangioma port wine stain raspberry mark of skin strawberry angioma strawberry birthmark strawberry haemangioma of skin strawberry hemangioma of skin strawberry mark of skin strawberry naevus strawberry naevus of skin strawberry nevi strawberry nevus strawberry nevus of skin strawberry nevus of skin (disorder) strawberry nevus of skin, nos
DOID	DOID:2725 DOID:471
UMLS	C0206733
MeSH	D018324
SNOMED-CT	SNOMEDCT_US_2016_09_01:402867006;SNOMEDCT_US_2016_09_01:254206003;SNOMEDCT_US_2016_09_01:56975005
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:23) C0019562 \| von hippel-lindau disease \| 3 C0019562 \| hippel-lindau disease \| 3 C0020542 \| pulmonary hypertension \| 3 C0019562 \| lindau disease \| 3 C0034951 \| refractive error \| 1 C0035305 \| retinal detachment \| 1 C0020538 \| hypertension \| 1 C0007134 \| renal cell carcinoma \| 1 C0009782 \| connective tissue disease \| 1 C0206721 \| inverted papillomas \| 1 C0002418 \| amblyopia \| 1 C0034091 \| pulmonary veno-occlusive disease \| 1 C0206138 \| crest syndrome \| 1 C0020255 \| hydrocephalus \| 1 C0031039 \| pericardial effusion \| 1 C0206721 \| inverted papilloma \| 1 C0015300 \| proptosis \| 1 C0011649 \| dermoid cyst \| 1 C0271051 \| macular edema \| 1 C0003857 \| arteriovenous malformation \| 1 C0034069 \| pulmonary fibrosis \| 1 C0011649 \| dermoid \| 1 C0012739 \| consumptive coagulopathy \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:92) 6405 \| SEMA3F \| DISEASES 5010 \| CLDN11 \| DISEASES 634 \| CEACAM1 \| DISEASES 3294 \| HSD17B2 \| DISEASES 7980 \| TFPI2 \| DISEASES 3199 \| HOXA2 \| DISEASES 56913 \| C1GALT1 \| DISEASES 113263 \| GLCCI1 \| DISEASES 6347 \| CCL2 \| DISEASES 6909 \| TBX2 \| DISEASES 30848 \| CTAG2 \| DISEASES 3050 \| HBZ \| DISEASES 182 \| JAG1 \| DISEASES 10894 \| LYVE1 \| DISEASES 5460 \| POU5F1 \| DISEASES 4001 \| LMNB1 \| DISEASES 7450 \| VWF \| DISEASES 5629 \| PROX1 \| DISEASES 5159 \| PDGFRB \| DISEASES 2324 \| FLT4 \| DISEASES 9172 \| MYOM2 \| DISEASES 2294 \| FOXF1 \| DISEASES 3791 \| KDR \| DISEASES 10664 \| CTCF \| DISEASES 2247 \| FGF2 \| DISEASES 8829 \| NRP1 \| DISEASES 100820829 \| MYZAP \| DISEASES 207 \| AKT1 \| DISEASES 5972 \| REN \| DISEASES 7220 \| TRPC1 \| DISEASES 890 \| CCNA2 \| DISEASES 5921 \| RASA1 \| DISEASES 2321 \| FLT1 \| DISEASES 170692 \| ADAMTS18 \| DISEASES 7070 \| THY1 \| DISEASES 760 \| CA2 \| DISEASES 10630 \| PDPN \| DISEASES 5364 \| PLXNB1 \| DISEASES 6786 \| STIM1 \| DISEASES 84168 \| ANTXR1 \| DISEASES 9723 \| SEMA3E \| DISEASES 3688 \| ITGB1 \| DISEASES 29071 \| C1GALT1C1 \| DISEASES 154 \| ADRB2 \| DISEASES 1051 \| CEBPB \| DISEASES 51162 \| EGFL7 \| DISEASES 1072 \| CFL1 \| DISEASES 947 \| CD34 \| DISEASES 7423 \| VEGFB \| DISEASES 3170 \| FOXA2 \| DISEASES 1537 \| CYC1 \| DISEASES 3039 \| HBA1 \| DISEASES 6605 \| SMARCE1 \| DISEASES 84876 \| ORAI1 \| DISEASES 7490 \| WT1 \| DISEASES 10810 \| WASF3 \| DISEASES 9547 \| CXCL14 \| DISEASES 10011 \| SRA1 \| DISEASES 23462 \| HEY1 \| DISEASES 1003 \| CDH5 \| DISEASES 7316 \| UBC \| DISEASES 2331 \| FMOD \| DISEASES 80781 \| COL18A1 \| DISEASES 2526 \| FUT4 \| DISEASES 5083 \| PAX9 \| DISEASES 5788 \| PTPRC \| DISEASES 23493 \| HEY2 \| DISEASES 642489 \| FKBP1C \| DISEASES 988 \| CDC5L \| DISEASES 7422 \| VEGFA \| DISEASES 26508 \| HEYL \| DISEASES 2022 \| ENG \| DISEASES 4855 \| NOTCH4 \| DISEASES 7010 \| TEK \| DISEASES 2280 \| FKBP1A \| DISEASES 6164 \| RPL34 \| DISEASES 174 \| AFP \| DISEASES 1052 \| CEBPD \| DISEASES 3481 \| IGF2 \| DISEASES 3702 \| ITK \| DISEASES 8831 \| SYNGAP1 \| DISEASES 4140 \| MARK3 \| DISEASES 8842 \| PROM1 \| DISEASES 6513 \| SLC2A1 \| DISEASES 4193 \| MDM2 \| DISEASES 641700 \| ECSCR \| DISEASES 4043 \| LRPAP1 \| DISEASES 4914 \| NTRK1 \| DISEASES 5228 \| PGF \| DISEASES 400550 \| FENDRR \| DISEASES 79104 \| MEG8 \| DISEASES 654321 \| SNORA75 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1404
Disease	capillary hemangioma
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:18) HP:0002092 \| Pulmonary artery hypertension \| 3 HP:0001698 \| Pericardial effusions \| 1 HP:0040049 \| Macular edema \| 1 HP:0000822 \| Hypertension \| 1 HP:0000541 \| Detached retina \| 1 HP:0007917 \| Tractional retinal detachment \| 1 HP:0100026 \| Arteriovenous malformation \| 1 HP:0000969 \| Dropsy \| 1 HP:0003256 \| Coagulopathy \| 1 HP:0005584 \| Renal cell carcinoma \| 1 HP:0012531 \| Pain \| 1 HP:0012329 \| Angioblastoma \| 1 HP:0000520 \| Anterior bulging of the globe of eye \| 1 HP:0000238 \| Nonsyndromal hydrocephalus \| 1 HP:0002206 \| Pulmonary fibrosis \| 1 HP:0012721 \| Venous malformations \| 1 HP:0002105 \| Hemoptysis \| 1 HP:0000646 \| Wandering eyes \| 1

Disease ID	1404
Disease	capillary hemangioma
Manually Symptom	(Waiting for update.)
Text Mined Symptom	(Waiting for update.)

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)
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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.)

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