ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
DRS1
http://purl.bioontology.org/ontology/OMIM/180700
FETAL FACE SYNDROME
ROBINOW DWARFISM
ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES
C4551475
C0265205
3p21-p14
WNT5A
http://purl.bioontology.org/ontology/OMIM/MTHU019018
http://purl.bioontology.org/ontology/OMIM/MTHU000231
http://purl.bioontology.org/ontology/OMIM/MTHU009593
http://purl.bioontology.org/ontology/OMIM/MTHU003093
http://purl.bioontology.org/ontology/OMIM/MTHU031455
http://purl.bioontology.org/ontology/OMIM/MTHU009605
http://purl.bioontology.org/ontology/OMIM/MTHU000191
http://purl.bioontology.org/ontology/OMIM/MTHU005403
http://purl.bioontology.org/ontology/OMIM/MTHU000263
http://purl.bioontology.org/ontology/OMIM/MTHU002155
http://purl.bioontology.org/ontology/OMIM/MTHU005790
http://purl.bioontology.org/ontology/OMIM/MTHU002079
http://purl.bioontology.org/ontology/OMIM/MTHU000576
http://purl.bioontology.org/ontology/OMIM/MTHU004213
http://purl.bioontology.org/ontology/OMIM/MTHU009595
http://purl.bioontology.org/ontology/OMIM/MTHU002029
http://purl.bioontology.org/ontology/OMIM/MTHU009607
http://purl.bioontology.org/ontology/OMIM/MTHU000185
http://purl.bioontology.org/ontology/OMIM/MTHU009598
http://purl.bioontology.org/ontology/OMIM/MTHU000583
http://purl.bioontology.org/ontology/OMIM/MTHU001061
http://purl.bioontology.org/ontology/OMIM/MTHU000514
http://purl.bioontology.org/ontology/OMIM/MTHU000512
http://purl.bioontology.org/ontology/OMIM/MTHU036357
http://purl.bioontology.org/ontology/OMIM/MTHU002153
http://purl.bioontology.org/ontology/OMIM/MTHU005092
http://purl.bioontology.org/ontology/OMIM/MTHU001627
http://purl.bioontology.org/ontology/OMIM/MTHU000259
http://purl.bioontology.org/ontology/OMIM/MTHU000560
http://purl.bioontology.org/ontology/OMIM/MTHU001789
http://purl.bioontology.org/ontology/OMIM/MTHU000041
http://purl.bioontology.org/ontology/OMIM/MTHU001172
http://purl.bioontology.org/ontology/OMIM/MTHU000073
http://purl.bioontology.org/ontology/OMIM/MTHU034630
http://purl.bioontology.org/ontology/OMIM/MTHU006883
http://purl.bioontology.org/ontology/OMIM/MTHU031450
http://purl.bioontology.org/ontology/OMIM/MTHU005290
http://purl.bioontology.org/ontology/OMIM/MTHU007202
http://purl.bioontology.org/ontology/OMIM/MTHU000265
http://purl.bioontology.org/ontology/OMIM/MTHU010264
http://purl.bioontology.org/ontology/OMIM/MTHU000575
http://purl.bioontology.org/ontology/OMIM/MTHU067377
http://purl.bioontology.org/ontology/OMIM/MTHU009601
http://purl.bioontology.org/ontology/OMIM/MTHU001611
http://purl.bioontology.org/ontology/OMIM/MTHU009600
http://purl.bioontology.org/ontology/OMIM/MTHU000268
http://purl.bioontology.org/ontology/OMIM/MTHU067378
http://purl.bioontology.org/ontology/OMIM/MTHU000133
http://purl.bioontology.org/ontology/OMIM/MTHU009863
http://purl.bioontology.org/ontology/OMIM/MTHU000603
http://purl.bioontology.org/ontology/OMIM/MTHU015010
http://purl.bioontology.org/ontology/OMIM/MTHU036366
http://purl.bioontology.org/ontology/OMIM/MTHU000324
http://purl.bioontology.org/ontology/OMIM/MTHU009606
http://purl.bioontology.org/ontology/OMIM/MTHU009594
http://purl.bioontology.org/ontology/OMIM/MTHU001753
http://purl.bioontology.org/ontology/OMIM/MTHU000066
http://purl.bioontology.org/ontology/OMIM/MTHU064964
http://purl.bioontology.org/ontology/OMIM/MTHU000264
http://purl.bioontology.org/ontology/OMIM/MTHU004047
http://purl.bioontology.org/ontology/OMIM/MTHU010000
http://purl.bioontology.org/ontology/OMIM/MTHU009599
http://purl.bioontology.org/ontology/OMIM/MTHU009604
http://purl.bioontology.org/ontology/OMIM/MTHU009597
http://purl.bioontology.org/ontology/OMIM/MTHU000094
Phenotype description, molecular basis known.
180700
3
pound
Caused by mutation in the wingless-type MMTV integration site family, member 5A gene (WNT5A, 164975.0001) [MOLECULAR BASIS]
See also autosomal recessive Robinow syndrome (268310) [MISCELLANEOUS]
T047
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