MORM syndrome
medical condition
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MORM syndrome
Summary
MORM syndrome is a developmental defect during embryogenesis[1].
Key Facts
- MORM syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- MORM syndrome's instance of is recorded as rare disease[3].
- MORM syndrome's instance of is recorded as class of disease[4].
- MORM syndrome is a type of autosomal recessive disease[5].
- MORM syndrome is a type of syndromic obesity[6].
- MORM syndrome is a type of hereditary retinal dystrophy[7].
- MORM syndrome's symptoms and signs is recorded as intellectual disability[8].
- MORM syndrome's symptoms and signs is recorded as obesity[9].
- MORM syndrome's symptoms and signs is recorded as fundus dystrophy[10].
- MORM syndrome's symptoms and signs is recorded as micropenis[11].
- MORM syndrome's genetic association is recorded as INPP5E[12].
- MORM syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_75858[13].