Phenotypes for disease #05842 (RRS1 (Robinow, autosomal recessive syndrome, type 1 (RRS1)), OMIM:268310)

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Individual ID     
0000305427 - - Short stature [-5, 43 standard deviation (SD) score] and low weight (-3. 75 SD score), high forehead, broad wide nasal bone, upturned nose with anteverted nares, long philtrum and tented lips, telecanthus, hypertelorism, low set ears, macrocephaly and a triangular-fish mouth, pectus excavatum, mesomelic shortening of forearm, broad thumbs and other fingers, clinodactyly in left hand, syndactyly ing the second and third toes of the right foot and right cleft hand with absence of third finger. External genitalia revealed micropenis, retractile palpable testis and scrotal hypoplasia. Incomplete bladder duplication Familial, autosomal recessive 02y? - - - Juliana Mazzeu 00413454
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