PORPHYRIA, ACUTE HEPATIC, DIGENIC

OMIM®:

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PORPHYRIA, ACUTE HEPATIC, DIGENIC
PORPHYRIA, ACUTE HEPATIC, DIGENIC

MedGen
C4016013[conceptid] (1)
MedGen
"POLYMICROGYRIA WITHOUT VASCULAR-TYPE EHLERS-DANLOS SYNDROME"[Dis... (1)
"POLYMICROGYRIA WITHOUT VASCULAR-TYPE EHLERS-DANLOS SYNDROME"[Disease/phenotype] AND "OMIM"[submitter]
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ClinVar
"POLYCYSTIC OVARY SYNDROME, SUSCEPTIBILITY TO"[Disease/phenotype]... (0)
"POLYCYSTIC OVARY SYNDROME, SUSCEPTIBILITY TO"[Disease/phenotype] AND "OMIM"[submitter]
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ClinVar
"POLYCYSTIC LIVER DISEASE 4 WITH KIDNEY CYSTS"[Disease/phenotype]... (1)
"POLYCYSTIC LIVER DISEASE 4 WITH KIDNEY CYSTS"[Disease/phenotype] AND "OMIM"[submitter]
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ClinVar

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