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Hereditary chronic pancreatitis
1 OMIM reference -
5 associated genes
152 connected diseases
No signs/symptoms info
Disease Type of connection
Tropical pancreatitis
Cystic fibrosis
Congenital bilateral absence of vas deferens
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Behavioral variant of frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Amyotrophic lateral sclerosis
Hereditary nonpolyposis colon cancer
Autosomal dominant Emery-Dreifuss muscular dystrophy
X-linked non-syndromic intellectual deficit
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Early-onset autosomal dominant Alzheimer disease
Nuclear cataract
Spinocerebellar ataxia type 12
Alpha-1-antitrypsin deficiency
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Adult-onset distal myopathy due to VCP mutation
Angelman syndrome
Chronic myeloid leukemia
Distal 22q11.2 microdeletion syndrome
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Spastic paraplegia - Paget disease of bone
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Distal hereditary motor neuropathy type 2
CLN4B disease
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Congenital alpha2 antiplasmin deficiency
Cerebellar ataxia - hypogonadism
Juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
Acrokeratosis verruciformis of Hopf
Atypical Gaucher disease due to saposin C deficiency
Autosomal dominant hypocalcemia
Autosomal dominant spastic paraplegia type 13
CLN11 disease
Catecholaminergic polymorphic ventricular tachycardia
Congenital analbuminemia
Darier disease
Encephalopathy due to prosaposin deficiency
Extraskeletal myxoid chondrosarcoma
Familial gastric cancer
Familial hypocalciuric hypercalcemia type 2
Gastric linitis plastica
Hereditary motor and sensory neuropathy, Okinawa type
Hereditary sensory and autonomic neuropathy type 1
Infantile Krabbe disease
Intestinal epithelial dysplasia
Kostmann syndrome
Late-onset autosomal recessive medullary cystic kidney disease
Metachromatic leukodystrophy, adult form
Metachromatic leukodystrophy, juvenile form
Metachromatic leukodystrophy, late infantile form
Papillary or follicular thyroid carcinoma
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Primary CD59 deficiency
Severe X-linked mitochondrial encephalomyopathy
Severe combined immunodeficiency due to DNA-PKcs deficiency
Spastic paraplegia-optic atrophy-neuropathy syndrome
Unverricht-Lundborg disease
X-linked Charcot-Marie-Tooth disease type 4
X-linked Emery-Dreifuss muscular dystrophy
Pulverulent cataract
APC-related attenuated familial adenomatous polyposis
Annular epidermolytic ichthyosis
Atypical Werner syndrome
Autoimmune lymphoproliferative syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal dominant limb-girdle muscular dystrophy type 1F
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
Autosomal recessive Emery-Dreifuss muscular dystrophy
Autosomal recessive spastic paraplegia type 18
Autosomal recessive systemic lupus erythematosus
Baraitser-Winter syndrome
Blepharophimosis-intellectual deficit syndrome, MKB type
Brody myopathy
Cap myopathy
Charcot-Marie-Tooth disease type 2B1
Childhood-onset nemaline myopathy
Common variable immunodeficiency
Congenital fiber-type disproportion myopathy
Congenital muscular dystrophy due to LMNA mutation
Congenital reticular ichthyosiform erythroderma
Dedifferentiated liposarcoma
Desmoid tumor
Developmental malformations - deafness - dystonia
Diffuse palmoplantar keratoderma with painful fissures
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Epidermolytic ichthyosis
Epidermolytic palmoplantar keratoderma
FG syndrome type 1
Familial adenomatous polyposis due to 5q22.2 microdeletion
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial melanoma
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Familial renal amyloidosis due to Apolipoprotein AII variant
Focal palmoplantar keratoderma with joint keratoses
Gardner syndrome
Heart-hand syndrome, Slovenian type
Hutchinson-Gilford progeria syndrome
Inflammatory myofibroblastic tumor
Intermediate nemaline myopathy
Juvenile amyotrophic lateral sclerosis
Juvenile primary lateral sclerosis
Keratosis palmoplantaris striata
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Left ventricular noncompaction
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Neuralgic amyotrophy
Osteogenesis imperfecta type 2
Osteogenesis imperfecta type 3
Osteogenesis imperfecta type 4
Pachyonychia congenita
Primary biliary cirrhosis
Progeria-associated arthropathy
Recessive intellectual disability - motor dysfunction - multiple joint contractures
Severe dermatitis-multiple allergies-metabolic wasting syndrome
Turcot syndrome with polyposis
Well-differentiated liposarcoma
Wolfram syndrome
X-linked intellectual deficit with marfanoid habitus
Alpha-1-antichymotrypsin deficiency
Metaphyseal anadysplasia
Nance-Horan syndrome
Total congenital cataract
Autosomal dominant cutis laxa
Christianson syndrome
Congenital enteropathy due to enteropeptidase deficiency
Glycogen storage disease due to muscle phosphorylase kinase deficiency
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Netherton syndrome
Supravalvular aortic stenosis
Williams syndrome
(no synonyms)

Classification (Orphanet):
- Rare endocrine disease
- Rare gastroenterologic disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the digestive system -

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.