PedAM

Pediatric Disease Annotations & Medicines


	lipoma

Disease ID	318
Disease	lipoma
Definition	A benign tumor composed of fat cells (ADIPOCYTES). It can be surrounded by a thin layer of connective tissue (encapsulated), or diffuse without the capsule.
Synonym	[m]lipoma nos [m]lipoma nos (morphologic abnormality) fatty tumor fatty tumors lipoma (clinical) lipoma (disorder) lipoma [disease/finding] lipoma nos lipoma nos (disorder) lipoma of unspecified body site lipoma, benign lipoma, no icd-o subtype lipoma, no icd-o subtype (morphologic abnormality) lipoma, no international classification of diseases for oncology subtype lipoma, no international classification of diseases for oncology subtype (morphologic abnormality) lipoma, nos lipoma, unspecified site lipomas lipomata lipomatas tumor, fatty tumors, fatty
OMIM	OMIM:151900
DOID	DOID:3315
UMLS	C0023798
MeSH	D008067
SNOMED-CT	SNOMEDCT_US_2016_09_01:93163002
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:49) C0021933 \| intussusception \| 14 C0080178 \| spina bifida \| 3 C0023827 \| liposarcoma \| 3 C0080178 \| spinal dysraphism \| 3 C0003864 \| arthritis \| 2 C0040997 \| trigeminal neuralgia \| 2 C0027662 \| multiple endocrine neoplasia \| 2 C0014544 \| epilepsy \| 2 C0039144 \| syringomyelia \| 2 C0029408 \| osteoarthritis \| 2 C0152110 \| meralgia paresthetica \| 1 C0025267 \| multiple endocrine neoplasia type 1 \| 1 C0014544 \| epileptic seizure \| 1 C0023801 \| madelung's disease \| 1 C0023801 \| madelung disease \| 1 C0206634 \| myxoid liposarcoma \| 1 C0003615 \| appendicitis \| 1 C0010068 \| coronary artery disease \| 1 C0700594 \| radiculopathy \| 1 C0036202 \| sarcoidosis \| 1 C0024115 \| lung disease \| 1 C0016522 \| patent foramen ovale \| 1 C0149756 \| plantar fasciitis \| 1 C0018553 \| cowden syndrome \| 1 C0017168 \| esophageal reflux \| 1 C0021843 \| intestinal obstruction \| 1 C0023801 \| lipomatosis \| 1 C0020492 \| hyperostosis \| 1 C0023827 \| liposarcomas \| 1 C0085693 \| acute appendicitis \| 1 C0014544 \| epileptic seizures \| 1 C0041296 \| tuberculosis \| 1 C0032357 \| poland syndrome \| 1 C0041327 \| pulmonary tuberculosis \| 1 C0017525 \| giant cell tumour \| 1 C0019202 \| wilson disease \| 1 C0003872 \| psoriatic arthritis \| 1 C0017075 \| ganglioneuroma \| 1 C0040961 \| tricuspid regurgitation \| 1 C0017168 \| oesophageal reflux \| 1 C0017168 \| gastroesophageal reflux \| 1 C1318558 \| congenital melanocytic nevus \| 1 C0007286 \| carpal tunnel syndrome \| 1 C0011649 \| dermoid \| 1 C0025299 \| meningocele \| 1 C0023798 \| lipomas \| 1 C0021933 \| intestinal intussusception \| 1 C0018916 \| hemangioma \| 1 C1096063 \| intractable epilepsy \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) PTEN \| 5728 \| CTD_human
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:149) 8847 \| DLEU2 \| DISEASES 5837 \| PYGM \| DISEASES 2099 \| ESR1 \| DISEASES 7049 \| TGFBR3 \| DISEASES 7249 \| TSC2 \| DISEASES 4150 \| MAZ \| DISEASES 123263 \| MTFMT \| DISEASES 708 \| C1QBP \| DISEASES 4617 \| MYF5 \| DISEASES 8574 \| AKR7A2 \| DISEASES 63923 \| TNN \| DISEASES 968 \| CD68 \| DISEASES 9426 \| CDY2A \| DISEASES 57688 \| ZSWIM6 \| DISEASES 3110 \| MNX1 \| DISEASES 1160 \| CKMT2 \| DISEASES 2521 \| FUS \| DISEASES 2167 \| FABP4 \| DISEASES 57498 \| KIDINS220 \| DISEASES 23175 \| LPIN1 \| DISEASES 55226 \| NAT10 \| DISEASES 1019 \| CDK4 \| DISEASES 6302 \| TSPAN31 \| DISEASES 1144 \| CHRND \| DISEASES 1134 \| CHRNA1 \| DISEASES 4069 \| LYZ \| DISEASES 6009 \| RHEB \| DISEASES 5862 \| RAB2A \| DISEASES 7350 \| UCP1 \| DISEASES 10347 \| ABCA7 \| DISEASES 6855 \| SYP \| DISEASES 10000 \| AKT3 \| DISEASES 5290 \| PIK3CA \| DISEASES 5924 \| RASGRF2 \| DISEASES 3371 \| TNC \| DISEASES 7982 \| ST7 \| DISEASES 1998 \| ELF2 \| DISEASES 26297 \| SERGEF \| DISEASES 8620 \| NPFF \| DISEASES 7157 \| TP53 \| DISEASES 207 \| AKT1 \| DISEASES 167410 \| LIX1 \| DISEASES 4851 \| NOTCH1 \| DISEASES 26040 \| SETBP1 \| DISEASES 221895 \| JAZF1 \| DISEASES 5468 \| PPARG \| DISEASES 3815 \| KIT \| DISEASES 25865 \| PRKD2 \| DISEASES 117159 \| DCD \| DISEASES 1145 \| CHRNE \| DISEASES 6746 \| SSR2 \| DISEASES 51705 \| EMCN \| DISEASES 819 \| CAMLG \| DISEASES 1345 \| COX6C \| DISEASES 7248 \| TSC1 \| DISEASES 161742 \| SPRED1 \| DISEASES 10818 \| FRS2 \| DISEASES 5346 \| PLIN1 \| DISEASES 4665 \| NAB2 \| DISEASES 9085 \| CDY1 \| DISEASES 253175 \| CDY1B \| DISEASES 3037 \| HAS2 \| DISEASES 794 \| CALB2 \| DISEASES 3159 \| HMGA1 \| DISEASES 6199 \| RPS6KB2 \| DISEASES 947 \| CD34 \| DISEASES 81839 \| VANGL1 \| DISEASES 4026 \| LPP \| DISEASES 150696 \| PROM2 \| DISEASES 64388 \| GREM2 \| DISEASES 55342 \| STRBP \| DISEASES 5745 \| PTH1R \| DISEASES 64840 \| PORCN \| DISEASES 3039 \| HBA1 \| DISEASES 7791 \| ZYX \| DISEASES 5324 \| PLAG1 \| DISEASES 5499 \| PPP1CA \| DISEASES 3052 \| HCCS \| DISEASES 64764 \| CREB3L2 \| DISEASES 10196 \| PRMT3 \| DISEASES 27445 \| PCLO \| DISEASES 5501 \| PPP1CC \| DISEASES 4221 \| MEN1 \| DISEASES 219541 \| MED19 \| DISEASES 6622 \| SNCA \| DISEASES 23583 \| SMUG1 \| DISEASES 57496 \| MKL2 \| DISEASES 1368 \| CPM \| DISEASES 1180 \| CLCN1 \| DISEASES 285386 \| TPRG1 \| DISEASES 113675 \| SDSL \| DISEASES 8445 \| DYRK2 \| DISEASES 1102 \| RCBTB2 \| DISEASES 64218 \| SEMA4A \| DISEASES 253827 \| MSRB3 \| DISEASES 4763 \| NF1 \| DISEASES 93034 \| NT5C1B \| DISEASES 4311 \| MME \| DISEASES 800 \| CALD1 \| DISEASES 9851 \| KIAA0753 \| DISEASES 722 \| C4BPA \| DISEASES 2205 \| FCER1A \| DISEASES 910 \| CD1B \| DISEASES 262 \| AMD1 \| DISEASES 5654 \| HTRA1 \| DISEASES 64783 \| RBM15 \| DISEASES 257 \| ALX3 \| DISEASES 81030 \| ZBP1 \| DISEASES 5728 \| PTEN \| DISEASES 90550 \| MCU \| DISEASES 139596 \| UPRT \| DISEASES 5303 \| PIN4 \| DISEASES 7321 \| UBE2D1 \| DISEASES 57683 \| ZDBF2 \| DISEASES 10927 \| SPIN1 \| DISEASES 22921 \| MSRB2 \| DISEASES 64421 \| DCLRE1C \| DISEASES 2308 \| FOXO1 \| DISEASES 10186 \| LHFP \| DISEASES 116840 \| CNTROB \| DISEASES 4781 \| NFIB \| DISEASES 2315 \| MLANA \| DISEASES 192668 \| CYS1 \| DISEASES 203611 \| CDY2B \| DISEASES 5627 \| PROS1 \| DISEASES 196410 \| METTL7B \| DISEASES 6164 \| RPL34 \| DISEASES 116135 \| LRRC3B \| DISEASES 116372 \| LYPD1 \| DISEASES 389136 \| VGLL3 \| DISEASES 8091 \| HMGA2 \| DISEASES 4052 \| LTBP1 \| DISEASES 57703 \| CWC22 \| DISEASES 3481 \| IGF2 \| DISEASES 2260 \| FGFR1 \| DISEASES 1029 \| CDKN2A \| DISEASES 387836 \| CLEC2A \| DISEASES 9278 \| ZBTB22 \| DISEASES 79827 \| CLMP \| DISEASES 4193 \| MDM2 \| DISEASES 5515 \| PPP2CA \| DISEASES 5890 \| RAD51B \| DISEASES 6949 \| TCOF1 \| DISEASES 1649 \| DDIT3 \| DISEASES 51741 \| WWOX \| DISEASES 102723508 \| KANTR \| DISEASES 4566 \| MT-TK \| DISEASES 94161 \| SNORD46 \| DISEASES 26774 \| SNORD80 \| DISEASES
Locus	(Waiting for update.)

Disease ID	318
Disease	lipoma
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:47) HP:0002576 \| Intussusception \| 14 HP:0002664 \| Neoplasia \| 13 HP:0002144 \| Occult spinal dysraphism \| 5 HP:0002584 \| Intestinal hemorrhage \| 4 HP:0002239 \| Gastrointestinal hemorrhage \| 4 HP:0002414 \| Spina bifida \| 3 HP:0001274 \| Absent corpus callosum \| 3 HP:0010301 \| Spinal dysraphism \| 3 HP:0012034 \| Liposarcoma \| 3 HP:0100661 \| Trigeminal neuralgia \| 2 HP:0001369 \| Arthritis \| 2 HP:0002758 \| Osteoarthritis \| 2 HP:0001250 \| Seizures \| 2 HP:0001031 \| Subcutaneous lipoma \| 2 HP:0003396 \| Syringomyelia \| 2 HP:0100568 \| Endocrine neoplasia \| 2 HP:0006989 \| Dysplastic corpus callosum \| 1 HP:0011675 \| Arrhythmias \| 1 HP:0002094 \| Dyspnea \| 1 HP:0030710 \| Lipomeningocele \| 1 HP:0001297 \| Cerebral vascular events \| 1 HP:0001028 \| Strawberry mark \| 1 HP:0100565 \| Hydromyelia \| 1 HP:0030871 \| Facet joint arthrosis \| 1 HP:0002020 \| Heartburn \| 1 HP:0001655 \| Patent foramen ovale \| 1 HP:0001289 \| Confusion \| 1 HP:0005180 \| Tricuspid insufficiency \| 1 HP:0100600 \| Prepenile scrotum \| 1 HP:0005214 \| Bowel obstruction \| 1 HP:0002282 \| Heterotopias \| 1 HP:0100523 \| Hepatic abscess \| 1 HP:0002825 \| Coccygeal tail \| 1 HP:0100790 \| Hernia \| 1 HP:0004756 \| Ventricular tachycardia \| 1 HP:0001636 \| Tetrology of fallot \| 1 HP:0012268 \| Myxoid liposarcoma \| 1 HP:0003005 \| Ganglioneuroma \| 1 HP:0000969 \| Dropsy \| 1 HP:0001677 \| Coronary artery disease \| 1 HP:0000995 \| Beauty mark \| 1 HP:0030274 \| Extra scrotum \| 1 HP:0002539 \| Cortical dysplasia \| 1 HP:0002573 \| Bloody diarrhea \| 1 HP:0003077 \| Hyperlipidemia \| 1 HP:0100774 \| Hyperostosis \| 1 HP:0002435 \| Meningocele \| 1

Disease ID	318
Disease	lipoma
Manually Symptom	UMLS \| Name(Total Manually Symptoms:13) C2585575 \| recurrent abdominal pains C2127111 \| fluctuating hearing loss C2112237 \| posterior interosseous nerve palsy C1532393 \| nuchal-type fibroma C1412297 \| aicardi syndrome C0267467 \| colonic intussusception C0267373 \| intestinal bleeding C0235031 \| neurological symptoms C0205824 \| dedifferentiated liposarcoma C0158026 \| monoarthritis C0031038 \| pericardial cyst C0026266 \| mitral incompetence C0021933 \| intussusception
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:5) C0021933 \| intussusception \| 14 C0267373 \| intestinal bleeding \| 4 C0267467 \| colonic intussusception \| 3 C2112237 \| posterior interosseous nerve palsy \| 1 C0205824 \| dedifferentiated liposarcoma \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:1)
snpId	pubmedId	geneId	geneSymbol	diseaseId	sourceId	sentence	score	Year	geneSymbol_dbSNP	CHROMOSOME	POS	REF	ALT
rs121913529	25928347	3845	KRAS	umls:C0023798	BeFree	We conclude that KENS, the intraneural Schwann cell proliferation and the lipoma in this individual were caused by a postzygotic and mosaic activating c.35G > A (p.Gly12Asp) KRAS mutation.	0.000271442	2015	KRAS	12	25245350	C	T,G,A

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:1)
CUI	ChemicalName	ChemicalID	CasRN	DiseaseName	DiseaseID	DirectEvidence	PubMedIDs
C0023798	hydromorphone	D004091	466-99-9	lipoma	MESH:D008067	marker/mechanism	24141031

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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