Phenotypes for disease #00870 (FGLDS1 (Feingold syndrome, type 1), OMIM:164280)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Individual ID     
0000280751 see paper; ..., variable phenotype (5 affected); esophageal atresia, tracheoesophageal fistula; microcephaly; toe syndactyly; clinodactyly (1/5) Feingold syndrome FGLDS1 Familial, autosomal dominant - - - - - Rafał Płoski 00386956
0000359491 Delayed speech and language development, Short stature, Microcephaly, Ptosis, Brachydactyly, Toe clinodactyly, Abnormality of the face, Narrow palate, Macrotia - - Isolated (sporadic) 01y - - - - Andreas Laner 00474698
0000359492 Delayed speech and language development, Short stature, Microcephaly, Ptosis, Brachydactyly, Toe clinodactyly, Abnormality of the face, Narrow palate, Macrotia - - Isolated (sporadic) 01y - - - - Andreas Laner 00474699
0000359586 see paper; ..., microcephaly (10m-OFC <3rd); mild generalized hypotonia; prominent metopic suture, ocular hypotelorism, low set ears, depressed nasal bridge, bilateral clinodactyly fifth fingers, cutaneous syndactyly multiple toes; bronchiolitis, otitis media, atopic dermatitis Feingold syndrome FGLDS1 Isolated (sporadic) 01y01m - - - - Johan den Dunnen 00474793
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