MORM syndrome
medical condition
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MORM syndrome
Summary
MORM syndrome is a developmental defect during embryogenesis[1]. It draws 1 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]
Key Facts
- MORM syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- MORM syndrome's instance of is recorded as rare disease[4].
- MORM syndrome's instance of is recorded as class of disease[5].
- MORM syndrome's subclass of is recorded as autosomal recessive disease[6].
- MORM syndrome's subclass of is recorded as syndromic obesity[7].
- MORM syndrome's subclass of is recorded as hereditary retinal dystrophy[8].
- MORM syndrome's MeSH descriptor ID is recorded as C536984[9].
- MORM syndrome's OMIM ID is recorded as 610156[10].
- MORM syndrome's symptoms and signs is recorded as intellectual disability[11].
- MORM syndrome's symptoms and signs is recorded as obesity[12].
- MORM syndrome's symptoms and signs is recorded as fundus dystrophy[13].
- MORM syndrome's symptoms and signs is recorded as micropenis[14].
- MORM syndrome's Orphanet ID is recorded as 75858[15].
- MORM syndrome's genetic association is recorded as INPP5E[16].
- MORM syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_75858[17].
- MORM syndrome's UMLS CUI is recorded as C1857802[18].
- MORM syndrome's GARD rare disease ID is recorded as 10121[19].
- MORM syndrome's Mondo ID is recorded as MONDO_0012423[20].
- MORM syndrome's Microsoft Academic ID is recorded as 2779317568[21].
- MORM syndrome's ICD-11 ID is recorded as 1027545274[22].
- MORM syndrome's UniProt disease ID is recorded as DI-02533[23].
Why It Matters
MORM syndrome draws 1 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]