Disease #05842 (RRS1 (Robinow, autosomal recessive syndrome, type 1 (RRS1)), OMIM:268310)

Official abbreviation RRS1
Name Robinow, autosomal recessive syndrome, type 1 (RRS1)
OMIM ID 268310
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene ROR2
Associated tissues -
Disease features -
Remarks -
Date created 2020-09-29 10:02:52 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00413454 patient PubMed: Demirkan 2022, Journal: Demirkan 2022 - M yes Turkey - - - - - RRS1 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 - ROR2 1 1 Juliana Mazzeu
00448526 patient PubMed: Yang 2024 - M no - - - - - - RRS1 - - ROR2 2 1 Juliana Mazzeu
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