Phenotypes for disease #00560 (MARTS1 (Martsolf syndrome, type 1), OMIM:212720)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000258530 see paper; ..., no intrauterine growth retardation, postnatal growth retardation; birth OF 34cm; postnatal microcephaly; no seizures; truncal hypotonia; limb spasticity and spastic cerebral palsy; 3y-speech; 3y-walking; congenital cataracts?, microphthalmia; brachycephaly; no distinct dysmorphic features, no maxillary retrusion or pouting lips; hirsutism; female no genital abnormalities/male micropenis, cryptorchidism; large ears; CT brain normal Martsolf syndrome Martsolf syndrome Familial, autosomal recessive - - - - - Johan den Dunnen 00363164
0000325600 High palate, Retrognathia, Hearing impairment, Cataract, Developmental cataract, Hypotelorism, Synophrys, Single transverse palmar crease, Dystonia - - Unknown 01y - - - - Andreas Laner 00435409
0000352832 - Martsolf syndrome MARTS1 Familial, autosomal recessive - - - - - Xuemei Tan 00467591
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