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5 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
7 OMIM references -
8 associated genes
10 signs/symptoms
Congenital pulmonary alveolar proteinosis
Narcolepsy-cataplexy

ABCA3 CTSH
CSF2RA HCRT
CSF2RB HLA-DQB1
SFTPB HLA-DRB1
SFTPC MOG
P2RY11
TNFSF4
ZNF365


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SFTPB
(0.52)
CTSH



Citations in the biomedical literature:


Congenital pulmonary alveolar proteinosis
ABCA3 CSF2RA CSF2RB SFTPB SFTPC
Narcolepsy-cataplexy
CTSH HCRT HLA-DQB1 HLA-DRB1 MOG P2RY11
TNFSF4 ZNF365



Congenital pulmonary alveolar proteinosis
Narcolepsy-cataplexy

Synonym(s):
- Congenital PAP

Synonym(s):
- GĂ©lineau disease

Classification (Orphanet):
- Rare genetic disease
- Rare respiratory disease
Classification (Orphanet):
- Rare neurologic disease

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: unknown

External references:
5 OMIM references -
No MeSH references
External references:
7 OMIM references -
1 MeSH reference: D009290

Narcolepsy-cataplexy

Very frequent
- Delirium / hallucination
- Muscle weakness / flaccidity
- Sleep and vigilance disorders
- Somnolence / hypersomnia / parasomnia
- Troubles of memory / amnesia / hypermnesia

Frequent
- Abnormal eye movements / oculomotor disorder
- Anomalies of eyes and vision

Occasional
- Collapse / sudden death / cardiac arrest / cardiorespiratory arrest
- Generalized obesity
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia


Congenital pulmonary alveolar proteinosis

(no data available)