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| created at |
2017-12-21 11:07:44 UTC |
| updated at |
2017-12-22 12:31:05 UTC |
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2 layers
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520,470 entries
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There is 0 pattern entry.
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Caused by mutation in the cartilage-associated protein gene (CRTAP, 605497.0001)
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DISO:OMIM |
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Heterozygous females may have gout and/or sensorineural deafness
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DISO:OMIM |
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MAFD4
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DISO:OMIM |
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BPAD
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DISO:OMIM |
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MAJOR AFFECTIVE DISORDER 4
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DISO:OMIM |
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MAJOR AFFECTIVE DISORDER 4
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DISO:MTH |
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Major Affective Disorder 4
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DISO:MSH |
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BIPOLAR AFFECTIVE DISORDER
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DISO:OMIM |
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Hypoplastic, bicornuate uterus
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DISO:OMIM |
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Caused by mutation in the homolog of the mouse stimulated by retinoic acid-6 gene (STRA6, 610745.0007)
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DISO:OMIM |
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Low-normal platelet count in carrier females
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DISO:OMIM |
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XERODERMA PIGMENTOSUM B/COCKAYNE SYNDROME
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DISO:OMIM |
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XPB/CS
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DISO:OMIM |
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XERODERMA PIGMENTOSUM B/COCKAYNE SYNDROME
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DISO:OMIM |
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Xeroderma Pigmentosum B-Cockayne Syndrome
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DISO:MSH |
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