Phenotype Annotations Click to see Annotation Detail View
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Phenotype Annotations Click to see Annotation Detail View
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Database | Acc Id | Source(s) |
ClinVar | RCV001143930 | CLINVAR |
RCV001143931 | CLINVAR | |
RCV001143932 | CLINVAR | |
RCV001143933 | CLINVAR | |
RCV001143934 | CLINVAR | |
RCV001143935 | CLINVAR | |
RCV001145829 | CLINVAR | |
dbSNP (RS) | rs762349019 | CLINVAR |
MedGen | C0086543 | CLINVAR |
C0344539 | CLINVAR | |
C0344559 | CLINVAR | |
C1842031 | CLINVAR | |
C1867155 | CLINVAR | |
C3714873 | CLINVAR | |
CN239168 | CLINVAR | |
NCBI Gene | PITX2 | CLINVAR |
OMIM | 137600 | CLINVAR |
180500 | CLINVAR | |
180550 | CLINVAR | |
601542 | CLINVAR | |
604229 | CLINVAR | |
SNOMED CT | 204153003 | CLINVAR |