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X-linked intellectual deficit, Porteous type
1 associated gene
No signs/symptoms info
COMMON GENES: 1
X-linked intellectual deficit, Sutherland-Haan type
1 associated gene
No signs/symptoms info
X-linked intellectual deficit, Porteous type
X-linked intellectual deficit, Sutherland-Haan type

PQBP1
(UniProt - OMIM)
 PQBP1
(UniProt - OMIM)

COMMON
GENES 		PQBP1


Citations in the biomedical literature:


X-linked intellectual deficit, Porteous type
PQBP1
X-linked intellectual deficit, Sutherland-Haan type



X-linked intellectual deficit, Porteous type
X-linked intellectual deficit, Sutherland-Haan type

Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: x-linked recessive
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.