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| Pituitary hormone deficiency v1.12 | KMT2A | chirag patel reviewed gene: KMT2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 35617449; Phenotypes: Wiedemann-Steiner syndrome, MONDO:0011518; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Pituitary hormone deficiency v1.12 | chirag patel Copied gene KMT2A from panel Hypertrichosis syndromes | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Pituitary hormone deficiency v1.12 | KMT2A |
chirag patel gene: KMT2A was added gene: KMT2A was added to Pituitary hormone deficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: KMT2A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: KMT2A were set to Wiedemann-Steiner syndrome, MIM# 605130 AD |
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