Source: HPO

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
disease 0.400 strong 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
group 0.400 strong 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome
disease 0.130 1.000 0 0 2013 2017
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
Globe retraction and deviation on adduction
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1845112
Disease: Hyperkyphosis
Hyperkyphosis
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
Neurogenic muscle atrophy, especially in the lower limbs
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1843367
Disease: Poor school performance
Poor school performance
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1842587
Disease: Sensory axonal neuropathy
Sensory axonal neuropathy
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1850189
Disease: Large pinnae
Large pinnae
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1857483
Disease: Decreased palmar creases
Decreased palmar creases
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1857130
Disease: Hypoplastic mandible condyle
Hypoplastic mandible condyle
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1856872
Disease: Down-sloping shoulders
Down-sloping shoulders
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1855353
Disease: Fixed facial expression
Fixed facial expression
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1855350
Disease: Inferior vermis hypoplasia
Inferior vermis hypoplasia
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1855285
Disease: Protruding ear
Protruding ear
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1854301
Disease: Motor delay
Motor delay
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1850656
Disease: Firm muscles
Firm muscles
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1839798
Disease: Long nose
Long nose
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1839764
Disease: Broad flat nasal bridge
Broad flat nasal bridge
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
Primitive reflexes (palmomental, snout, glabellar)
phenotype 0.100 0 0
Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
piezo type mechanosensitive ion channel component 2 0.573 0.655 2.3E-06
CUI: C1305420
Disease: Prominent ear
Prominent ear
phenotype 0.100 0 0