Phenotypes for disease #00833 (MRXSC (Mental retardation, X-linked, syndromic 15 (Cabezas type)), OMIM:300354)

12 entries on 1 page. Showing entries 1 - 12.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Birth_Details     

Protein     

Owner     

Individual ID     
0000020209 - - - Familial - - - - - - Anneke Vulto-van Silfhout 00022455
0000020210 - - - Familial - - - - - - Anneke Vulto-van Silfhout 00022454
0000020211 - - - Familial - - - - - - Anneke Vulto-van Silfhout 00022453
0000020212 - - - Familial - - - - - - Anneke Vulto-van Silfhout 00022456
0000020213 - - - Isolated (sporadic) - - - - - - Anneke Vulto-van Silfhout 00022452
0000020214 - - - Isolated (sporadic) - - - - - - Anneke Vulto-van Silfhout 00022451
0000020215 - - - Isolated (sporadic) - - - - - - Anneke Vulto-van Silfhout 00022450
0000020216 - - - Isolated (sporadic) - - - - - - Anneke Vulto-van Silfhout 00022449
0000020217 - - - Familial, X-linked recessive - - - - - - Anneke Vulto-van Silfhout 00022448
0000020218 - - - Familial, X-linked recessive - - - - - - Anneke Vulto-van Silfhout 00022447
0000020219 - - - Familial, X-linked recessive - - - - - - Anneke Vulto-van Silfhout 00022446
0000306590 Intellectual disability, mild, Sleep disturbance, Lipoma, EEG abnormality, Seizure - - Familial, X-linked recessive 11y - - - - - Andreas Laner 00414789
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