Search Ontology:
Human Disease
Renpenning syndrome
- Term ID
- DOID:0060179
- Synonyms
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- Golabi-Ito-Hall syndrome
- Sutherland-Haan X-linked mental retardation syndrome
- syndromic X-linked mental retardation 8
- X-linked intellectual disability due to PQBP1 mutations
- X-linked intellectual disability, Renpenning type
- X-linked mental retardation Renpenning type
- X-linked mental retardation with spastic diplegia
- Definition
- An intellectual disability that is characterized by small head size (microcephaly), long narrow face, short stature, small testes, and intellectual deficit which follows X-linked inheritance and presents most often in males. http://en.wikipedia.org/wiki/Renpenning%27s_syndrome
- References
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- ICD10CM:Q87.5
- MIM:309500
- ORDO:3242
- Ontology
- Human Disease ( DOID:0060179 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models