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Diseases
Genes (271)
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HMBS
Porphyria, Acute Intermittent
Aminolevulinic Acid Dehydratase Deficiency Porphyria
Variegate Porphyria
CPOX
Porphyria, Acute Intermittent
Aminolevulinic Acid Dehydratase Deficiency Porphyria
Hereditary Coproporphyria
Variegate Porphyria
UBR1
Johanson-Blizzard Syndrome
ASL
Argininosuccinic Aciduria
FRAS1
Fraser Syndrome 2
PPOX
Porphyria, Acute Intermittent
Aminolevulinic Acid Dehydratase Deficiency Porphyria
Hereditary Coproporphyria
Variegate Porphyria
FREM2
Fraser Syndrome 2
PMM2
Pmm2 Deficiency
ALAD
Porphyria, Acute Intermittent
Porphyria Due To Ala Dehydratase Deficiency
Aminolevulinic Acid Dehydratase Deficiency Porphyria
ESCO2
Sc Phocomelia Syndrome
PLEC
Epidermolysis Bullosa Simplex With Pyloric Atresia
ARX
Lissencephaly, X-Linked, 2
MED12
Ohdo Syndrome, X-Linked
GRIP1
Fraser Syndrome 2
MGP
Keutel Syndrome
ALG9
Gillessen-Kaesbach-Nishimura Syndrome
MYO18B
Klippel-Feil Syndrome 4, Autosomal Recessive, With Nemaline Myopathy And Facial Dysmorphism
ALX1
Frontonasal Dysplasia 3
CLPX
Protoporphyria, Erythropoietic, 2
HFE
Variegate Porphyria