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| Additional findings_Paediatric v0.2 | TPM2 | Zornitza Stark Added phenotypes Arthrogryposis multiplex congenita, distal for gene: TPM2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | TPM2 |
Zornitza Stark gene: TPM2 was added gene: TPM2 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene Mode of inheritance for gene: TPM2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: TPM2 were set to Nemaline myopathy |
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