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: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		group 0.430 None 1.000 0 0 2009 2019
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0856863
Disease: Broad-based gait
Broad-based gait 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0848558
Disease: Hypospadias
Hypospadias 		disease 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0426891
Disease: Broad thumbs
Broad thumbs 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0426415
Disease: Large nose
Large nose 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0424711
Disease: Orbital separation diminished
Orbital separation diminished 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0423867
Disease: Fine hair
Fine hair 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		disease 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C1837463
Disease: Narrow face
Narrow face 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C1858085
Disease: Malar flattening
Malar flattening 		disease 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C1849089
Disease: Broad forehead
Broad forehead 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C1848207
Disease: Poor speech
Poor speech 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0423110
Disease: Downward slant of palpebral fissure
Downward slant of palpebral fissure 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0349588
Disease: Short stature
Short stature 		phenotype 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0026034
Disease: Microstomia
Microstomia 		disease 0.100 None 0 0
Entrez Id: 51132
Gene Symbol: RLIM
RLIM 		ring finger protein, LIM domain interacting 0.686 0.500 0.99
CUI: C0025990
Disease: Micrognathism
Micrognathism 		disease 0.100 None 0 0