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: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C1386091
Disease: Acromicria
Acromicria 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0265287
Disease: Acromicric Dysplasia
Acromicric Dysplasia 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C4024780
Disease: Almond-shaped palpebral fissure
Almond-shaped palpebral fissure 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C4551485
Disease: Clinodactyly
Clinodactyly 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C1844527
Disease: Clitoral hypoplasia
Clitoral hypoplasia 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C1837108
Disease: Decreased muscle mass
Decreased muscle mass 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0034012
Disease: Delayed Puberty
Delayed Puberty 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0013336
Disease: Dwarfism
Dwarfism 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C1867873
Disease: Failure to thrive in infancy
Failure to thrive in infancy 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C1849923
Disease: Generalized hypopigmentation
Generalized hypopigmentation 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0556280
Disease: Gross motor impairment
Gross motor impairment 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0020490
Disease: Hyperopia
Hyperopia 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0020505
Disease: Hyperphagia
Hyperphagia 		phenotype 0.100 None 0 0