Phenotypes for disease #03558 (PRLTS3;DFNB81 (Perrault syndrome, type 3 (PRLTS3; DFNB81)), OMIM:614129)

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000043005 see paper; ..., Perrault syndrome (PRTLS) - - Familial, autosomal recessive - - - - - Leigh Demain 00056386
0000061345 sensorineural hearing loss (HP:0000407) psychomotor retardation (HP:0001263) white matter abnormalities, periventricular (MRI) (HP:0002500), (HP:0002518) spastic ataxia (HP:0002497) sensorimotor neuropathy (HP:0007141) stunted growth (HP:0001510) - - Familial, autosomal recessive - - 01y 1y - Tom Theunissen 00081707
0000061346 Sensorineural hearing loss (HP:0000407) epilepsy, seizures (HP:0001250) White matter affected (MRI), periventricular, (HP:0002500),(HP:0002518) spastic ataxia (HP:0002497) psychomotor retardation (HP:0001263) autism (HP:0000717) - - Familial, autosomal recessive <01y 01y 01y - - Tom Theunissen 00081706
0000061347 sensorineural hearingloss (HP:0000408) psychomotor delay (HP:0001263) spastic diplegia (HP:0001264) microcephaly (HP:0000252) growth delay (HP:0001510) - - Familial, autosomal recessive - - 03y 3y - Tom Theunissen 00081708
0000325459 Hearing impairment, Intellectual disability, Neurodevelopmental delay, Short stature, Spasticity - - Familial, autosomal recessive 17y - - - - Andreas Laner 00435262
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