Van Maldergem syndrome
Human disease
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Van Maldergem syndrome
Summary
Van Maldergem syndrome is a developmental defect during embryogenesis[1].
Key Facts
- Van Maldergem syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- Van Maldergem syndrome's instance of is recorded as rare disease[3].
- Van Maldergem syndrome's instance of is recorded as class of disease[4].
- Van Maldergem syndrome's subclass of is recorded as syndrome[5].
- Van Maldergem syndrome's subclass of is recorded as Pashayan syndrome[6].
- Van Maldergem syndrome's subclass of is recorded as autosomal recessive disease[7].
- Van Maldergem syndrome's MeSH descriptor ID is recorded as C536530[8].
- Van Maldergem syndrome's OMIM ID is recorded as 601390[9].
- Van Maldergem syndrome's KEGG ID is recorded as H01393[10].
- Van Maldergem syndrome's Disease Ontology ID is recorded as DOID:0060238[11].
- Van Maldergem syndrome's Orphanet ID is recorded as 314679[12].
- Van Maldergem syndrome's genetic association is recorded as FAT4[13].
- Van Maldergem syndrome's genetic association is recorded as DCHS1[14].
- Van Maldergem syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060238[15].
- Van Maldergem syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060238[16].
- Van Maldergem syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_314679[17].
- Van Maldergem syndrome's UMLS CUI is recorded as C1832390[18].
- Van Maldergem syndrome's GARD rare disease ID is recorded as 5456[19].
- Van Maldergem syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
- Van Maldergem syndrome's Mondo ID is recorded as MONDO_0017813[21].