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Prepros no me funciona Pc#

Hereditary Thrombophilia Due To Congenital Protein C Deficiency.

Prepros no me funciona Pc#

Autosomal Recessive Thrombophilia Due To Pc Deficiency.

Autosomal Recessive Thrombophilia Due To Congenital Protein C Deficiency.

Autosomal Recessive Protein C Deficiency.

Autosomal Recessive Thrombophilia Due To Protein C Deficiency.

Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Recessive.

Thrombophilia Due To Protein C Deficiency, Autosomal Recessive 1 4 6 99 101 109

Sea Urchin (Strongylocentrotus purpuratus).

Schistosome Parasite (Schistosoma mansoni).

Malaria Parasite (Plasmodium falciparum).

Green Algae (Chlamydomonas reinhardtii).

Fission Yeast (Schizosaccharomyces pombe).

Firmicute Bacteria (Streptococcus pneumoniae).

Filamentous fungi (Aspergillus nidulans).

Chromalveolata (Phytophthora infestans).

Beta proteobacteria (Neisseria meningitidis).

Baker's yeast (Saccharomyces cerevisiae).

Alpha proteobacteria (Wolbachia pipientis).

African malaria mosquito (Anopheles gambiae).

Actinobacteria (Mycobacterium tuberculosis).

Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.Īutosomal dominant Autosomal dominant form Autosomal dominant typeĪ mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele).Īutosomal recessive Autosomal recessive form Autosomal recessive predispositionĪny abnormality of the eye, including location, spacing, and intraocular abnormalities.Ībnormal eye Abnormality of the eye Eye diseaseĪny structural anomaly of a blood vessel (artery, arteriole, capillary, venule, or vein).Ībnormality of the nervous system Brain and/or spinal cord issue Neurologic abnormalities Neurological abnormality In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. MAP3K2-DT ERCC3 MAP3K2 AMMECR1L PROC WDR33 ENSG00000231731 RNU4-48P LIMS2 piR-36393-296Ī mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. NCOR1 ZNF10 FOXA2 TAL1 YBX1 TCF12 ATF4 HNF4A MEIS2 SP7 PROC lnc-IWS1-1 HSALNG0018621 ERCC3 MAP3K2 WDR33 AMMECR1L ENSG00000231731 SAP130ĬEBPA KLF11 MIER3 RXRA EBF1 KAT7 DRAP1 TEAD3 BCL6 CREM KLF6 YY1 CEBPA MXD4 KMT2B KDM6A KLF11 SAP130 FOXA2 HOMEZ