has material basis in germline mutation in disease has feature PQBP1 Microcephaly Narrow face Intellectual disability Short stature Decreased testicular size Renpenning syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/9285 https://www.malacards.org/card/renpenning_syndrome https://www.malacards.org/card/renpenning_syndrome_1 ICD9:759.89 GARD:0009509 OMIM:309500 X-linked intellectual disability with spastic diplegia intellectual disability, X-linked Renpenning type MONDO:0010653 RENS1 DOID:0060179 mental retardation, X-linked 55 MRXS3 X-linked intellectual disability syndromic 3 mental retardation, X-linked, syndromic 3 mental retardation, X-linked, syndromic 8 renpenning syndrome, X-linked recessive NCIT:C165533 MRXS8 X-linked intellectual disability, Renpenning type X-linked intellectual disability Renpenning type X-linked mental retardation syndromic 3 SCTID:699669001 Sutherland-Haan X-linked mental retardation syndrome mental retardation, X-linked, Renpenning type An X-linked syndrome characterized by intellectual deficiency, microcephaly, leanness and mild short stature. MEDGEN:208670 MESH:C537761 Golabi-Ito-Hall syndrome UMLS:C0796135 Orphanet:3242 mental retardation, X-linked, with spastic diplegia Renpenning syndrome 1 Sutherland-Haan syndrome mental retardation, X-linked Renpenning type Sutherland-Haan X-linked intellectual disability syndrome icd11.foundation:1415315699 X-linked intellectual disability due to PQBP1 mutations syndromic X-linked intellectual disability 8 Renpenning syndrome type 1 Renpenning syndrome multiple congenital anomalies/dysmorphic syndrome-intellectual disability obsolete syndromic anorectal malformation X-linked syndromic intellectual disability