Cytoscape Web
Click node...

Idiopathic CD4 lymphocytopenia
1 OMIM reference -
1 associated gene
28 connected diseases
No signs/symptoms info
Disease Type of connection
Cone rod dystrophy
T-B+ severe combined immunodeficiency due to CD3delta / CD3epsilon / CD3zeta
Multiple endocrine neoplasia type 1
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
Severe combined immunodeficiency due to LCK deficiency
Retinitis pigmentosa
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Congenital stationary night blindness
Late-onset autosomal recessive medullary cystic kidney disease
NPHP3-related Meckel-like syndrome
Renal-hepatic-pancreatic dysplasia
Senior-Loken syndrome
Amyotrophic lateral sclerosis
Chronic myeloid leukemia
Distal 22q11.2 microdeletion syndrome
Distal hereditary motor neuropathy type 2
Familial isolated dilated cardiomyopathy
Keratosis follicularis spinulosa decalvans
LIG4 syndrome
Lennox-Gastaut syndrome
Omenn syndrome
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Punctate palmoplantar keratoderma type 1
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
UNC119 Q13432604011
No signs/symptoms info available.