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Familial gastric cancer
1 OMIM reference -
2 associated genes
114 connected diseases
No signs/symptoms info
Disease Type of connection
Gastric linitis plastica
MUTYH-related attenuated familial adenomatous polyposis
Familial isolated dilated cardiomyopathy
Giant cell glioblastoma
Gliosarcoma
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Hepatocellular carcinoma, childhood-onset
Epidermolytic palmoplantar keratoderma
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Constitutional mismatch repair deficiency syndrome
Hereditary nonpolyposis colon cancer
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Pilomatrixoma
Lethal acantholytic epidermolysis bullosa
Naxos disease
Behavioral variant of frontotemporal dementia
Early-onset autosomal dominant Alzheimer disease
Progressive non-fluent aphasia
Semantic dementia
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Annular epidermolytic ichthyosis
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal dominant spastic paraplegia type 13
Autosomal recessive Emery-Dreifuss muscular dystrophy
Charcot-Marie-Tooth disease type 2B1
Congenital muscular dystrophy due to LMNA mutation
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Epidermolytic ichthyosis
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Heart-hand syndrome, Slovenian type
Hutchinson-Gilford progeria syndrome
Ichthyosis hystrix of Curth-Macklin
Keratosis palmoplantaris striata
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Left ventricular noncompaction
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Progeria-associated arthropathy
Very long chain acyl-CoA dehydrogenase deficiency
Alpha-crystallinopathy
Fatal infantile hypertonic myofibrillar myopathy
Posterior polar cataract
Zonular cataract
Charcot-Marie-Tooth disease type 4D
EEM syndrome
Hypotrichosis with juvenile macular degeneration
Autosomal dominant Charcot-Marie-Tooth disease type 2P
Alobar holoprosencephaly
Autosomal dominant macrothrombocytopenia
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Baraitser-Winter syndrome
Congenital bilateral absence of vas deferens
Cystic fibrosis
Familial papillary renal cell carcinoma
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Lobar holoprosencephaly
Male infertility with normal virilization due to meiosis defect
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Usher syndrome type 1
Intellectual deficit, X-linked, Turner type
Lethal congenital contracture syndrome type 3
1p36 deletion syndrome
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Bannayan-Riley-Ruvalcaba syndrome
Cone rod dystrophy
Cowden syndrome
Hartsfield-Bixler-Demyer syndrome
Hereditary breast and ovarian cancer syndrome
Isolated trigonocephaly
Juvenile polyposis of infancy
Kallmann syndrome
Lhermitte-Duclos disease
Macrocephaly-autism syndrome
Myeloid neoplasm associated with FGFR1 rearrangement
Normosmic congenital hypogonadotropic hypogonadism
Oligodontia
Osteoglophonic dwarfism
Papillary or follicular thyroid carcinoma
Pfeiffer syndrome type 1
Pilocytic astrocytoma
Proteus syndrome
Proteus-like syndrome
Retinitis pigmentosa
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
Septo-optic dysplasia
Shprintzen-Goldberg syndrome
Squamous cell carcinoma of head and neck
Uveal coloboma - cleft lip and palate - intellectual deficit
22q11.2 deletion syndrome
Monosomy 5p
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
Autoimmune lymphoproliferative syndrome with recurrent infections
Synonym(s):
- Familial stomach cancer
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CDH1 P12830192090
MUTYH Q9UIF7604933
No signs/symptoms info available.