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Idiopathic pulmonary fibrosis
1 OMIM reference -
11 associated genes
111 connected diseases
No signs/symptoms info
Disease Type of connection
Dyskeratosis congenita
Idiopathic aplastic anemia
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Lethal acantholytic epidermolysis bullosa
Hoyeraal-Hreidarsson syndrome
Keratosis palmoplantaris striata
Chronic respiratory distress with surfactant metabolism deficiency
Congenital pulmonary alveolar proteinosis
Desquamative interstitial pneumonia
Diffuse panbronchiolitis
Familial melanoma
Infant acute respiratory distress syndrome
Skin fragility-woolly hair-palmoplantar keratoderma syndrome
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Acute promyelocytic leukemia
Adult-onset distal myopathy due to VCP mutation
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Spastic paraplegia - Paget disease of bone
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Familial isolated dilated cardiomyopathy
Precursor T-cell acute lymphoblastic leukemia
Autosomal recessive nonsyndromic intellectual deficit
Early-onset autosomal dominant Alzheimer disease
Naxos disease
Cowden syndrome
Proteus syndrome
Epidermolysis bullosa simplex due to plakophilin deficiency
Annular epidermolytic ichthyosis
Autosomal dominant limb-girdle muscular dystrophy type 1E
Autosomal recessive limb-girdle muscular dystrophy due to desmin deficiency
Epidermolytic ichthyosis
Epidermolytic palmoplantar keratoderma
Ichthyosis hystrix of Curth-Macklin
Pulverulent cataract
Scapuloperoneal amyotrophy
Coats plus syndrome
Exfoliative ichthyosis
Anaplastic ependymoma
Common variable immunodeficiency
Leber congenital amaurosis
Senior-Loken syndrome
Cerebellar ataxia - hypogonadism
Spinocerebellar ataxia type 12
Generalized junctional epidermolysis bullosa, non-Herlitz type
Late-onset junctional epidermolysis bullosa
Localized junctional epidermolysis bullosa, non-Herlitz type
46,XY partial gonadal dysgenesis
Autosomal dominant Charcot-Marie-Tooth disease type 2N
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
B-cell chronic lymphocytic leukemia
Blepharophimosis-intellectual deficit syndrome, MKB type
Burkitt lymphoma
Charcot-Marie-Tooth disease type 2B2
Estrogen resistance syndrome
FG syndrome type 1
Fabry disease
Familial thoracic aortic aneurysm and aortic dissection
Frontotemporal dementia with motor neuron disease
Glycogen storage disease due to muscle beta-enolase deficiency
Hereditary nonpolyposis colon cancer
Hereditary sensory and autonomic neuropathy with spastic paraplegia
Isolated growth hormone deficiency type IA
Isolated growth hormone deficiency type IB
Isolated growth hormone deficiency type II
Joubert syndrome
Joubert syndrome with hepatic defect
Laron syndrome with immunodeficiency
Loeys-Dietz syndrome type 1
Marfan syndrome type 2
Meckel syndrome
Methylcobalamin deficiency type cblG
Papillary or follicular thyroid carcinoma
Pontocerebellar hypoplasia type 1
Pseudohypoaldosteronism type 2E
Pyogenic arthritis - pyoderma gangrenosum - acne
Senior-Boichis syndrome
Short stature due to growth hormone qualitative anomaly
X-linked intellectual deficit with marfanoid habitus
X-linked non-syndromic intellectual deficit
Dowling-Degos disease
Epidermolysis bullosa simplex with circinate migratory erythema
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex, Dowling-Meara type
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type
Localized epidermolysis bullosa simplex
Hamel cerebro-palato-cardiac syndrome
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
X-linked intellectual deficit, Golabi-Ito-Hall type
X-linked intellectual deficit, Porteous type
X-linked intellectual deficit, Sutherland-Haan type
Chronic myeloid leukemia
Pachyonychia congenita
Precursor B-cell acute lymphoblastic leukemia
Autoimmune lymphoproliferative syndrome
CLN2 disease
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
Immunodeficiency due to an early component of complement deficiency
Reticular dysgenesis
- Usual interstitial pneumonia

Classification (Orphanet):
- Rare respiratory disease

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

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: D054990

No signs/symptoms info available.