MDP syndrome
human disease
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MDP syndrome
Summary
MDP syndrome is a head and neck disease[1]. It draws 12 Wikipedia views per month (head_and_neck_disease category, ranking #48 of 92).[2]
Key Facts
- MDP syndrome's instance of is recorded as head and neck disease[3].
- MDP syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- MDP syndrome's instance of is recorded as rare disease[5].
- MDP syndrome's instance of is recorded as class of disease[6].
- MDP syndrome's subclass of is recorded as Hearing loss with craniofacial syndromes[7].
- MDP syndrome's subclass of is recorded as progeroid syndrome[8].
- MDP syndrome's subclass of is recorded as syndromic genetic deafness[9].
- MDP syndrome's Commons category is recorded as MDP syndrome[10].
- MDP syndrome's OMIM ID is recorded as 615381[11].
- MDP syndrome's Orphanet ID is recorded as 363649[12].
- MDP syndrome's genetic association is recorded as POLD1[13].
- MDP syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_363649[14].
- MDP syndrome's UMLS CUI is recorded as C3715192[15].
- MDP syndrome's ICD-10-CM is recorded as E34.8[16].
- MDP syndrome's GARD rare disease ID is recorded as 10989[17].
- MDP syndrome's Mondo ID is recorded as MONDO_0014157[18].
- MDP syndrome's Microsoft Academic ID is recorded as 2781123483[19].
- MDP syndrome's Microsoft Academic ID is recorded as 2911031850[20].
- MDP syndrome's UniProt disease ID is recorded as DI-03863[21].
Why It Matters
MDP syndrome draws 12 Wikipedia views per month (head_and_neck_disease category, ranking #48 of 92).[2]