Phenotypes for disease #01445 (CWS1 (Cowden syndrome, type 1 (CWS1)), OMIM:158350)

20 entries on 1 page. Showing entries 1 - 20.
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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     
0000045620 melanoma (HP:0002861), trichilemmoma (HP:0012844), breast adenocarcinoma, no thyroid abormality (-HP:000082), glioblastoma (HP:0100843) - - Familial, autosomal dominant - - - - - Johan den Dunnen 00059031
0000045621 trichilemmoma (HP:0012844), no breast adenocarcinoma, thyroid follicular adenoma, no CNS abnormality - - Familial, autosomal dominant - - - - - Johan den Dunnen 00059032
0000045622 trichilemmoma (HP:0012844), no breast adenocarcinoma, thyroid multinodular Goiter, macrocephaly (HP:0000256) - - Familial, autosomal dominant - - - - - Johan den Dunnen 00059033
0000045623 trichilemmoma (HP:0012844), breast fibroadenoma/hamartoma, no thyroid abormality (-HP:000082), macrocephaly (HP:0000256) lehrmitte-Duclos - - Familial, autosomal dominant - - - - - Johan den Dunnen 00059034
0000045624 trichilemmoma (HP:0012844), breast adenocarcinoma, thyroid follicular carcinoma, no CNS abnormality - - Familial, autosomal dominant - - - - - Johan den Dunnen 00059035
0000052461 - - - Unknown - - - - - Jean-Pierre Bayley 00072770
0000061485 typical mucocutaneous lesions, begnin thyroid lesions, hamartomas polys, glycogenic acanthosis, lipovascular lesions, macrocephaly (HP:0000256) - - Familial, autosomal dominant 43y - - 43y - Michel Longy 00081841
0000061486 Typical mucocutaneous lesions, begnin thyroid lesions,begnin breast lesions,hamartomas polyps,glycogenic acanthosis, lipovascular lesions, macrocephaly, uterine fibromas - - Familial, autosomal dominant 62y - - 62y - Michel Longy 00081842
0000144248 Cowden syndrome - - Unknown - - - - - Stephanie Baert-Desurmont 00183544
0000144249 Cowden syndrome - - Unknown - - - - - Stephanie Baert-Desurmont 00183545
0000144250 Cowden syndrome - - Unknown - - - - - Stephanie Baert-Desurmont 00183546
0000144251 Cowden syndrome - - Unknown - - - - - Stephanie Baert-Desurmont 00183547
0000144253 Cowden syndrome - - Unknown - - - - - Stephanie Baert-Desurmont 00183549
0000144254 Cowden syndrome - - Unknown - - - - - Stephanie Baert-Desurmont 00183550
0000144255 Cowden syndrome - - Unknown - - - - - Stephanie Baert-Desurmont 00183551
0000144256 Cowden syndrome - - Unknown - - - - - Stephanie Baert-Desurmont 00183552
0000144257 Cowden syndrome - - Unknown - - - - - Stephanie Baert-Desurmont 00183553
0000144258 Cowden syndrome - - Unknown - - - - - Stephanie Baert-Desurmont 00183554
0000274244 Macrocephaly, Abnormality of the face, Global developmental delay, Abnormal facial shape, Mild global developmental delay, Neurodevelopmental delay, Increased head circumference - - Unknown - - - - - Andreas Laner 00380394
0000351561 Intellectual disability, Deafness, Macrocephaly, Cleft palate - - Unknown - - - - - Juliana Mazzeu 00466174
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