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Familial capillary hemangioma
1 OMIM reference -
2 associated genes
56 connected diseases
No signs/symptoms info
Disease Type of connection
GAPO syndrome
Juvenile myelomonocytic leukemia
Milroy disease
Hepatocellular carcinoma, childhood-onset
Autosomal dominant nonsyndromic intellectual deficit
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Split hand-split foot malformation
Hereditary mixed polyposis syndrome
Knobloch syndrome
Capillary malformation - arteriovenous malformation
Parkes Weber syndrome
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Seckel syndrome
Familial advanced sleep-phase syndrome
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Acute promyelocytic leukemia
Familial papillary renal cell carcinoma
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Familial pancreatic carcinoma
Familial prostate cancer
Hereditary breast and ovarian cancer syndrome
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Primary peritoneal carcinoma
Chronic mucocutaneous candidiasis
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Sorsby's fundus dystrophy
Susceptibility to viral and mycobacterial infections
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Autosomal dominant centronuclear myopathy
Autosomal dominant hypocalcemia
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Autosomal dominant macrothrombocytopenia
Congenital pulmonary alveolar proteinosis
Desmoid tumor
Familial hypocalciuric hypercalcemia type 2
Familial multiple nevi flammei
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Fetal and neonatal alloimmune thrombocytopenia
Glanzmann thrombasthenia
LEOPARD syndrome
Noonan syndrome
PLCG2-associated antibody deficiency and immune dysregulation
Sturge-Weber syndrome
Dyssegmental dysplasia, Silverman-Handmaker type
Schwartz-Jampel syndrome
(no synonyms)

Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
ANTXR1 Q9H6X2606410
KDR P35968191306
No signs/symptoms info available.