Phenotypes for disease #03491 (FANCP (Fanconi anemia, complementation group P (FANCP)), OMIM:613951)

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000017783 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00020020
0000017784 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00020021
0000017785 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00020022
0000017786 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00020023
0000017787 - - - Isolated (sporadic) - - - - - Arleen D. Auerbach 00020024
0000017788 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00020025
0000017789 prenatal dystrophy, short stature, hypoplasia right thumb, microcephaly, hyperpigmentation, cafÈ-au-lait, vitiligo, hypothyreoidism - - Familial, autosomal recessive - - - - - Beatrice Schuster 00020026
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