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PROTEIN INTERACTIONS: 1
35 OMIM references -
25 associated genes
2 signs/symptoms
Hereditary persistence of fetal hemoglobin - sickle cell disease
X-linked non-syndromic intellectual deficit

HBB ACSL4
HBG1 AGTR2
HBG2 ALG13
KLF1 ARHGEF6
ARX
DLG3
FTSJ1
GDI1
HCFC1
IL1RAPL1
IQSEC2
MAGT1
MECP2
MED12
MID2
PAK3
RAB39B
RPS6KA3
SYP
TSPAN7
UPF3B
ZNF41
ZNF674
ZNF711
ZNF81


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HBB
(0.49)
UPF3B



Citations in the biomedical literature:


Hereditary persistence of fetal hemoglobin - sickle cell disease
HBB HBG1 HBG2 KLF1
X-linked non-syndromic intellectual deficit
ACSL4 AGTR2 ALG13 ARHGEF6 ARX DLG3
FTSJ1 GDI1 HCFC1 IL1RAPL1 IQSEC2 MAGT1
MECP2 MED12 MID2 PAK3 RAB39B RPS6KA3
SYP TSPAN7 UPF3B ZNF41 ZNF674 ZNF711
ZNF81



Hereditary persistence of fetal hemoglobin - sickle cell disease
X-linked non-syndromic intellectual deficit

Synonym(s):
- HPFH - sickle cell disease

Synonym(s):
- X-linked non-specific intellectual deficit

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

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: no data available
Type of inheritance: x-linked recessive

External references:
No OMIM references
No MeSH references
External references:
35 OMIM references -
No MeSH references

X-linked non-syndromic intellectual deficit

Very frequent
- Intellectual deficit / mental / psychomotor retardation / learning disability
- X-linked recessive inheritance



Hereditary persistence of fetal hemoglobin - sickle cell disease

(no data available)