Phenotype #0000059586

Individual ID 00079873
Associated disease SHFM6
Phenotype details Affected individuals in this large consanguineous family showed variable prototypes of split hand foot malformation
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Irfan Ullah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Irfan Ullah
Date created 2016-08-21 09:01:05 +02:00 (CEST)
Date last edited 2016-08-22 16:37:48 +02:00 (CEST)

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