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MCID: KRS001
MIFTS: 6
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Krauss Herman Holmes Syndrome
Categories:
Eye diseases, Fetal diseases, Rare diseases
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MalaCards integrated aliases for Krauss Herman Holmes Syndrome:
Name: Krauss Herman Holmes Syndrome
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71
Classifications:
Orphanet: 58
Rare eye diseases
Developmental anomalies during embryogenesis |
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MalaCards based summary :
Krauss Herman Holmes Syndrome, is also known as telecanthus, hypertelorism, strabismus, and pes cavus syndrome. Affiliated tissues include eye.
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MalaCards organs/tissues related to Krauss Herman Holmes Syndrome:40
Eye
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Search
GEO
for disease gene expression data for Krauss Herman Holmes Syndrome.
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