FANCONI ANEMIA, COMPLEMENTATION GROUP C
General Information (adopted from Orphanet):
Synonyms, Signs: |
FANCONI PANCYTOPENIA, TYPE 3 FACC FA3 FAC FANCC |
Number of Symptoms | 38 |
OrphanetNr: | |
OMIM Id: |
227645
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ICD-10: |
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UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
Autosomal recessive inheritance [Omim] |
Age of onset: |
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Disease classification (adopted from Orphanet):
Parent Diseases: | No data available. |
Symptom Information:
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(HPO:0000085) | Horseshoe kidney | 39 / 7739 | ||||
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(HPO:0000028) | Cryptorchidism | 347 / 7739 | ||||
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(HPO:0000104) | Renal agenesis | 68 / 7739 | ||||
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(HPO:0000815) | Hypergonadotropic hypogonadism | 48 / 7739 | ||||
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(HPO:0000081) | Duplicated collecting system | 16 / 7739 | ||||
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(HPO:0012210) | Abnormal renal morphology | 18 / 7739 | ||||
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(HPO:0000086) | Ectopic kidney | 29 / 7739 | ||||
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(HPO:0000568) | Microphthalmia | 183 / 7739 | ||||
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(HPO:0000252) | Microcephaly | 832 / 7739 | ||||
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(HPO:0000486) | Strabismus | 576 / 7739 | ||||
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(HPO:0000365) | Hearing impairment | 539 / 7739 | ||||
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(HPO:0000598) | Abnormality of the ear | 98 / 7739 | ||||
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(HPO:0001249) | Intellectual disability | 1089 / 7739 | ||||
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(HPO:0001172) | Abnormality of the thumb | 103 / 7739 | ||||
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(HPO:0009777) | Absent thumb | 31 / 7739 | ||||
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(HPO:0009778) | Short thumb | 50 / 7739 | ||||
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(HPO:0009943) | Complete duplication of thumb phalanx | 8 / 7739 | ||||
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(HPO:0003974) | Absent radius | 26 / 7739 | ||||
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(HPO:0004322) | Short stature | 1232 / 7739 | ||||
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(HPO:0001518) | Small for gestational age | 107 / 7739 | ||||
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(HPO:0001017) | Anemic pallor | 5 / 7739 | ||||
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(HPO:0000957) | Cafe-au-lait spot | 84 / 7739 | ||||
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(HPO:0000978) | Bruising susceptibility | 123 / 7739 | ||||
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(HPO:0001000) | Abnormality of skin pigmentation | 105 / 7739 | ||||
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(HPO:0030680) | Abnormality of cardiovascular system morphology | 355 / 7739 | ||||
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(HPO:0001892) | Abnormal bleeding | 85 / 7739 | ||||
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(HPO:0001873) | Thrombocytopenia | 224 / 7739 | ||||
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(HPO:0001876) | Pancytopenia | 89 / 7739 | ||||
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(HPO:0001896) | Reticulocytopenia | 12 / 7739 | ||||
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(HPO:0001875) | Neutropenia | 83 / 7739 | ||||
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(HPO:0001909) | Leukemia | 46 / 7739 | ||||
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(HPO:0001903) | Anemia | 289 / 7739 | ||||
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(HPO:0003214) | Prolonged G2 phase of cell cycle | 5 / 7739 | ||||
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(HPO:0003213) | Deficient excision of UV-induced pyrimidine dimers in DNA | 5 / 7739 | ||||
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(HPO:0003220) | Abnormality of chromosome stability | 98 / 7739 | ||||
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(OMIM) | Hyperpigmentation | 24 / 7739 | ||||
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(OMIM) | Duplicated kidney | 4 / 7739 | ||||
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(OMIM) | Chromosomal breakage induced by diepoxybutane (DEB), and mitomycin C | 3 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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Additional Information:
Description: (OMIM) |
Fanconi anemia is a clinically and genetically heterogeneous disorder that causes genomic instability. Characteristic clinical features include developmental abnormalities in major organ systems, early-onset bone marrow failure, and a high predisposition to cancer. The cellular hallmark of FA ... |
Molecular genetics OMIM |
Strathdee et al. (1992) and Gavish et al. (1992) identified a missense mutation in the FANCC gene in the Fanconi anemia complementation group C cell line HSC536N (613899.0001). Approximately 25% of patients with Fanconi anemia have ... |