Entry Search - 136352 153100

Search: '136352 153100 (Search in: MIM number)'

Results: 2 entries.

* 136352. FMS-LIKE TYROSINE KINASE 4; FLT4
Cytogenetic location: 5q35.3, Genomic coordinates (GRCh38): 5:180,601,506-180,650,298
Matching terms: 136352
► Gene-Phenotype Relationships ► ICD+ ► Links

Gene-Phenotype Relationships
Location	Phenotype	Phenotype MIM number	Inheritance	Phenotype mapping key
5q35.3	Congenital heart defects, multiple types, 7	618780	AD	3
	Hemangioma, capillary infantile, somatic	602089		3
	Lymphatic malformation 1	153100	AD	3

▲ Close

Links
Testing GTR	Genome Ensembl NCBI Genome Viewer UCSC Genome Browser	DNA Ensembl (MANE Select) NCBI RefSeq NCBI RefSeq (MANE Select) UCSC Genome Browser	Protein HPRD Human Protein Atlas NCBI Protein UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG MARRVEL Monarch NCBI Gene UCSC	Clinical Resources ClinGen Validity MedlinePlus Genetics GTR	Variation ClinVar DECIPHER gnomAD GWAS Catalog GWAS Central HGMD NHLBI EVS PharmGKB	Animal Models Alliance Genome FlyBase IMPC MARRVEL MGI Mouse Gene MMRRC NCBI Orthologs OrthoDB Wormbase Gene WBGene00006894 WBGene00006897 ZFin	Cellular Pathways KEGG Reactome

▲ Close

ICD+
SNOMEDCT: 399889006

▲ Close

# 153100. LYMPHATIC MALFORMATION 1; LMPHM1
Cytogenetic location: 5q35.3
Matching terms: 153100
► Phenotype-Gene Relationships ► Phenotypic Series ► ICD+ ► Links

Phenotype-Gene Relationships
Location	Phenotype	Phenotype MIM number	Inheritance	Phenotype mapping key	Gene/Locus	Gene/Locus MIM number
5q35.3	Lymphatic malformation 1	153100	AD	3	FLT4	136352

▲ Close

Lymphatic malformation - PS153100 - 14 Entries

Location	Phenotype	Inheritance	Phenotype mapping key	Phenotype MIM number	Gene/Locus	Gene/Locus MIM number
1p34.2	Lymphatic malformation 11	AD	3	619401	TIE	600222
1q42.13	Lymphatic malformation 3	AD	3	613480	GJC2	608803
2q32.1	?Lymphatic malformation 8	AR	3	618773	CALCRL	114190
4q34.3	Lymphatic malformation 4	AD	3	615907	VEGFC	601528
5q35.3	Lymphatic malformation 1	AD	3	153100	FLT4	136352
6q16.2-q22.1	Lymphatic malformation 2	AD	2	611944	LMPHM2	611944
7q22.1	Lymphatic malformation 7	AD	3	617300	EPHB4	600011
7q31.1-q31.2	Lymphatic malformation 12	AR	3	620014	MDFIC	614511
8p23.1	Lymphatic malformation 10	AD	3	619369	ANGPT2	601922
13q14.3	Lymphatic malformation 13	AR	3	620244	THSD1	616821
16q24.3	Lymphatic malformation 6	AR	3	616843	PIEZO1	611184
21q22.2	Lymphatic malformation 14	AD	3	620602	ERG	165080
22q13.31	Lymphatic malformation 9	AD	3	619319	CELSR1	604523
Not Mapped	Lymphatic malformation 5	AD		153200	LMPHM5	153200

▲ Close

Links
Testing GTR EuroGentest	Clinical Resources Clinical Trials EuroGentest Gene Reviews Genetic Alliance MedlinePlus Genetics GTR OrphaNet	Animal Models Alliance Genome MGI Mouse Phenotype Wormbase Disease Ontology

▲ Close

ICD+
SNOMEDCT: 399889006 ORPHA: 79452 DO: 0070210

▲ Close

Search: 136352 153100 (Search in: MIM number)

Results: 2 entries.

* 136352. FMS-LIKE TYROSINE KINASE 4; FLT4
Cytogenetic location: 5q35.3, Genomic coordinates (GRCh38): 5:180,601,506-180,650,298
Matching terms: 136352

# 153100. LYMPHATIC MALFORMATION 1; LMPHM1
Cytogenetic location: 5q35.3
Matching terms: 153100

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM^® and Online Mendelian Inheritance in Man^® are registered trademarks of the Johns Hopkins University.
Copyright^® 1966-2025 Johns Hopkins University.
Printed: March 5, 2025