All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
07166 TYMAS Tayoun-Maawali syndrome 621184 AR - - FBXO22 - failure to thrive (HP:0001508) (0.87), intrauterine growth restriction (HP:0001511) (0.73), short stature (HP:0004322) (0.67), decreased body weight (HP:0004325) (0.60), neurodevelopmental delay (HP:0012758) (0.867), microcephaly (HP:0011451) (0.733), muscular hypotonia (HP:0001252) (0.67), seizures (HP:0001250) (0.53), generalized hypotonia (HP:0001290) (0.53), intellectual disability (HP:0001249) (0.47), poor suck (HP:0002033) (0.40), abnormal craniofacial shape (HP:0001999) (0.80), depressed nasal bridge (HP:0005280) (0.60), high forehead (HP:0000348) (0.53), hypertelorism (HP:0000316) (0.47)
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